CD HORIZON SPINAL SYSTEM
Report
- Report Number
- 1030489-2019-01003
- Event Type
- Injury
- Date Received
- September 11, 2019
- Report Date
- September 11, 2019
- Manufacturer
- MDT SOFAMOR DANEK PUERTO RICO MFG
- Product Code
- KWP
- PMA / PMN Number
- SEE H10
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NL
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
THE FOLLOWING PRODUCTS HAVE BEEN USED IN THE SURGERY: PART# 75446540; 510K# K042025; UDI# (B)(4); QTY# 2 PART# 75446545; 510K# K042025; UDI# (B)(4); QTY# 4 PART# 75446550; 510K# K042025; UDI# (B)(4); QTY# 1 PART# 75447545; 510K# K042025; UDI# (B)(4); QTY# 2 PART# 75447550; 510K# K042025; UDI# (B)(4); QTY# 2 PART# 75447555; 510K# K042025; UDI# (B)(4); QTY# 1 ALTHOUGH IT IS UNKNOWN WHETHER THESE PRODUCTS CAUSED OR CONTRIBUTED TO THE REPORTED EVENT, WE ARE FILLING THIS MDR FOR NOTIFICATION PURPOSE. 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.
IT WAS REPORTED VIA POST-OPERATIVE CLINICAL STUDY (WITH MINIMUM 12 MONTHS FOLLOW-UP) INVOLVING 155 PATIENTS WITH SPONDYLOLISTHESIS (103 PATIENTS), DEGENERATIVE DISC DISEASE (29 PATIENTS), STENOSIS (15 PATIENTS), RETROLISTHESIS (2 PATIENTS), DEGENERATION OF FACETS (3 PATIENTS) AND 3 DIAGNOSED WITH SPONDYLOLYSIS. IT WAS OBSERVED THAT SCREWS MIGRATED IN TEN PATIENTS. AS A RESULT OF THAT THE PATIENTS UNDERWENT REVISION SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 785175 | CD HORIZON SPINAL SYSTEM | APPLIANCE, FIXATION, SPINAL INTERLAMINAL | KWP | MDT SOFAMOR DANEK PUERTO RICO MFG | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Required Intervention |