510(k) K021025 ยท MQP Spinal Vertebral Body Replacement Device
MODIFICATION TO HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL XX-YYY-ZZZZ
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, May 20, 2002 |
| Received | Mar 29, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021025
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.