| Brand Name | CD HORIZON SOLERA 5.5/6.0 |
| Common Device Name | SCREWDRIVER |
| Manufacturer (Section D) |
| MEDTRONIC SOFAMOR DANEK USA, INC. |
| 4340 swinea rd |
| memphis TN 38118 |
|
| Manufacturer (Section G) |
| MEDTRONIC SOFAMOR DANEK USA, INC. |
| 4340 swinea rd |
|
| memphis TN 38118 |
|
| Manufacturer Contact |
|
justin
ellis
|
| 1800 pyramid place |
| memphis, TN 38132
|
|
+1(763)526-5677
|
|
| MDR Report Key | 50685123 |
| Report Number | 3003120897-2026-01537 |
| Device Sequence Number | 12091069 |
| Product Code |
HXX
|
| UDI-Device Identifier | 00643169043640 |
| Combination Product (Y/N) | N |
| Initial Reporter State | KY |
| Initial Reporter Country | US |
| PMA/510(K) Number | Exempt |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
User Facility |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/09/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Health Professional
|
| Device Model Number | 5584111 |
| Device Catalogue Number | 5584111 |
| Device Lot Number | SW20E029 |
| Was Device Available for Evaluation? |
Yes
|
| Date Returned to Manufacturer | 08/17/2026 |
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 08/18/2026 |
| Initial Report FDA Received Date | 09/09/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
Yes
|
| Date Device Manufactured | 06/16/2020 |
| Is the Device Labeled for Single Use? (Y/N) |
No
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Reuse
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|