INFUSE BONE GRAFT
Report
- Report Number
- 1030489-2010-00718
- Event Type
- Injury
- Date Received
- May 28, 2010
- Date of Event
- December 7, 2008
- Report Date
- April 28, 2010
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC.
- Product Code
- NEK
- PMA / PMN Number
- P000058
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
(B) (4). LITERATURE ARTICLE CITATION: ACOSTA F. PATIENT SATISFACTION AND RADIOGRAPHIC OUTCOMES AFTER LUMBAR SPINAL FUSION WITHOUT ILIAC CREST BONE GRAFT OR TRANSVERSE PROCESS FUSION" IN THE JOURNAL OF CLINICAL NEUROSCIENCE (2009; 16: 1184-1187); (10.1016/J.JOCN.2008.12.006). A REVIEW OF THE CERTIFICATES OF ANALYSIS AND PACKING LIST FOR THE INFUSE BONE GRAFT WAS NOT POSSIBLE WITHOUT ADDITIONAL DEVICE INFORMATION. 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. PRODUCTS FROM MULTIPLE MANUFACTURERS WERE IMPLANTED DURING THE PROCEDURE. ALTHOUGH IT IS UNKNOWN IF ANY OF THE DEVICES CONTRIBUTED TO THE REPORTED EVENT, WE ARE FILING THIS MDR FOR NOTIFICATION PURPOSES.
IT WAS REPORTED THAT TWO PATIENTS UNDERWENT A LAMINECTOMY FOLLOWED BY POSTERIOR SPINAL FUSION USING PEDICLE SCREW-ROD FIXATION. THE PATIENT ALSO UNDERWENT ANTERIOR LUMBAR INTERBODY FUSION (ALIF) USING RHBMP-2/ACS. THE PATIENTS DEVELOPED DEEP VEIN THROMBOSIS PERIOPERATIVELY. NO INTERVENTIONS WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INFUSE BONE GRAFT | INFUSE BONE GRAFT | NEK | MEDTRONIC SOFAMOR DANEK USA, INC. | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other | EXPLANT:| EXPLANT:| IMPLANT:| ROD| IMPLANT:| PEDICLE SCREW |