510(k) K072597 ยท MQV Filler, Bone Void, Calcium Compound
PRO-DENSE CORE DECOMPRESSION PROCEDURE KIT
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Oct 15, 2007 |
| Received | Sep 14, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072597
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.