Devices › Thoracolumbosacral pedicle screw system
Device brand name · Thoracolumbosacral pedicle screw system
CD HORIZON SOLERA Spinal System: medical device reports filed with FDA
320 reports name it, 2016–2026. Manufacturer given most often on reports: Mdt Sofamor Danek Puerto Rico Mfg. Product code NKB.
- 320
- device reports naming the brand
- 0% of all MAUDE reports · about 31 a year
- 68
- reports, 12 months to August 2026
- 33 in the 12 months before
- 62.2%
- classified as malfunction
- 41.2% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 320 reports that name the brand "CD HORIZON SOLERA Spinal System" (thoracolumbosacral pedicle screw system), received between March 2016 and August 2026; the manufacturer given most often on reports is Mdt Sofamor Danek Puerto Rico Mfg. Spellings of one product vary from report to report.
68 reports arrived in the 12 months to August 2026, up 106% from 33 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (62.2%) and injury (37.8%); across all thoracolumbosacral pedicle screw system reports (product code NKB) death is recorded in 0.3% and malfunction in 41.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are material deformation (22.8%), break (17.8%) and device dislodged or dislocated (10.3%). The patient problems coded most often are pain, device embedded in tissue or plaque and post operative wound infection. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 24,738 reports carrying product code NKB. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Material deformation | 73 | 22.8% | 5.5% |
| Breakthe device broke | 57 | 17.8% | 21.4% |
| Device dislodged or dislocated | 33 | 10.3% | 4.4% |
| Loosening of implant not related to bone-ingrowth | 30 | 9.4% | 2.8% |
| Failure to align | 21 | 6.6% | 0.6% |
| Mechanics altered | 21 | 6.6% | 0.3% |
| Migration or expulsion of device | 21 | 6.6% | 4.6% |
| Device slipped | 14 | 4.4% | 6% |
| Migrationthe device moved from where it was placed | 14 | 4.4% | 6.1% |
| Mechanical problema mechanical problem | 9 | 2.8% | 1.6% |
| Material fragmentation | 8 | 2.5% | 0.8% |
| Loose or intermittent connection | 6 | 1.9% | 4.6% |
| Metal shedding debris | 6 | 1.9% | 0.4% |
| Detachment of device or device componentpart of the device came off | 4 | 1.3% | 2.8% |
| Device damaged by another device | 4 | 1.3% | 0.2% |
| Mechanical jam | 4 | 1.3% | 0.6% |
| Product quality problem | 4 | 1.3% | 0.1% |
| Malposition of device | 3 | 0.9% | 1.1% |
| Manufacturing, packaging or shipping problem | 3 | 0.9% | 0% |
| Crackthe device cracked | 2 | 0.6% | 0.4% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Painpain, site not specified | 35 | 10.9% |
| Device embedded in tissue or plaque | 6 | 1.9% |
| Post operative wound infection | 4 | 1.3% |
| Failure of implant | 3 | 0.9% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 2 | 0.6% |
| Nonunion/delayed-union bone fracture | 2 | 0.6% |
| Blood loss | 1 | 0.3% |
| Bone fracture(s) | 1 | 0.3% |
| Discomfortdiscomfort | 1 | 0.3% |
| Headachehead pain | 1 | 0.3% |
| Inadequate osseointegration | 1 | 0.3% |
| Metal related pathology | 1 | 0.3% |
| Neuropathy | 1 | 0.3% |
| Numbnessnumbness | 1 | 0.3% |
| Sleep dysfunction | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | CD HORIZON SOLERA Spinal System | Product code NKB | All MAUDE reports |
|---|---|---|---|
| Reports | 320 | 24,738 | 26,136,888 |
| Share of that pool | — | 1.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 3 | 9 |
| Classified as injury | 37.8% | 58.1% | 36.2% |
| Classified as malfunction | 62.2% | 41.2% | 62.3% |
| Filed by the manufacturer | 100% | 99.2% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code NKB
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| CD HORIZON Spinal System | 9,787 | 634 | 0.3% |
| Ti Matrix Locking Cap | 489 | 0 | 1.2% |
| Blocker | 456 | 0 | 0% |
| Nuvasive Reline System | 468 | 8 | 1.5% |
| Single-Inner Setscrew | 454 | 19 | 0% |
| Closure Top | 440 | 27 | 0% |
| CD HORIZON SOLERA VOYAGER Spinal System | 775 | 216 | 0.1% |
| 5 5 Exp Verse Unitized Set Scr | 309 | 11 | 0% |
| Open Implant Closure Top | 277 | 0 | 0% |
| Unknown Mono/Polyaxial Screws | 390 | 0 | 0% |
| Verse Correction Key | 288 | 3 | 0% |
| Xia 3 Titanium Blocker | 340 | 7 | 0% |
| Mis Single Inner Setscw | 209 | 9 | 0.5% |
| Unknown_Spine_Product | 596 | 24 | 0% |
| Ti 12-Point Nut-11mm | 174 | 0 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about CD HORIZON SOLERA Spinal System reports
How many FDA reports name CD HORIZON SOLERA Spinal System?
320 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 68 in the latest 12 months.
What kinds of events are reported?
malfunction (62.2%) and injury (37.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
material deformation (22.8%), break (17.8%), device dislodged or dislocated (10.3%), loosening of implant not related to bone-ingrowth (9.4%) and failure to align (6.6%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that CD HORIZON SOLERA Spinal System was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.