INFUSE BONE GRAFT
Report
- Report Number
- 1030489-2013-02159
- Event Type
- Injury
- Date Received
- June 11, 2013
- Report Date
- November 28, 2016
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC
- Product Code
- NEK
- PMA / PMN Number
- P000058
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- ATTORNEY
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.
IT WAS REPORTED BY A NON-MEDICAL PROFESSIONAL THAT ON THE PATIENT UNDERWENT A PROCEDURE FOR ANTERIOR CERVICAL FUSION AT C4-C5 USING RHBMP-2. SUBSEQUENTLY, THE PATIENT WAS ALLEGEDLY DIAGNOSED WITH ECTOPIC BONE GROWTH, AN INFLAMMATORY REACTION TO RHBMP-2/ACS, CHRONIC PAIN, AND ADDITIONAL SURGERIES.
IT WAS REPORTED THAT ON (B)(6) 2008 THE PATIENT UNDERWENT ANTERIOR CERVICAL DECOMPRESSION AND FUSION, WITH INSTRUMENTATION AND PLACEMENT OF INTERBODY PEEK GRAFT, C4-5. PREOPERATIVE DIAGNOSIS: C4-5 HERNIATED NUCLEUS PULPOSUS. PER-OP NOTES: ¿UNTIL A NERVE HOOK COULD BE EASILY PASSED ALONG THE COURSE OF EACH NERVE ROOT. THE INTERSPACE WAS SIZED TO A 6-MM GRAFT, AND A 6-MM POLYETHER-ETHER-KETONE GRAFT WAS FILLED WITH BONE MORPHOGENETIC PROTEIN SPONGES AND PLACED IN THE DISK INTERSPACE. A ANTERIOR CERVICAL PLATE WAS AFFIXED TO THE ANTERIOR CERVICAL SPINE WITH 13-MM FIXED ANGLE SCREWS IN ACCORDANCE WITH THE TECHNIQUE MANUAL.¿
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 262711 | INFUSE BONE GRAFT | FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET | NEK | MEDTRONIC SOFAMOR DANEK USA, INC | NA | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 33 YR | Required Intervention |