510(k) K973056 ยท DZL Screw, Fixation, Intraosseous
BONE GRAFT SCREW SYSTEM
| Applicant | Bicon, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Nov 12, 1997 |
| Received | Aug 15, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973056
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.