CD HORIZON SPINAL SYSTEM
Report
- Report Number
- 1030489-2012-02200
- Event Type
- Malfunction
- Date Received
- November 14, 2012
- Date of Event
- November 13, 2012
- Report Date
- December 19, 2012
- Manufacturer
- MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS
- Product Code
- NKB
- PMA / PMN Number
- K102555
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SF
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4): NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT.
IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
ANALYSIS OF THE RETURNED DEVICE SHOWS THAT NO PRE-EXISTING DEFECT HAS BEEN IDENTIFIED AT THE LEVEL OF THE DAMAGES. THE DAMAGES OF THE MAS AND THE SETSCREWS ARE CONSISTENT WITH THE CROSS-THREADING OF THE SETSCREWS. CROSS-THREADING MAY HAPPEN WHEN THE SURGEON TRIES TO ENGAGE THE SETSCREW ON THE BONE SCREW HEAD ONCE PUSHING THE ROD WITH THE SETSCREW.
THE DEVICE HAS BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION. ANALYSIS RESULTS ARE NOT AVAILABLE AT THE TIME OF THIS REPORT. A FOLLOW-UP REPORT WILL BE SENT WHEN THE ANALYSIS IS COMPLETE.
IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN SPINAL PROCEDURE. DURING THE PROCEDURE IT WAS REPORTED THAT THE SCREW BROKE AND STRIPPED THE SET SCREW. NO FURTHER DETAILS ARE KNOWN AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CD HORIZON SPINAL SYSTEM | ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE | NKB | MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS | NA | H12F1350 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |