510(k) K012908 ยท DZL Screw, Fixation, Intraosseous
BIOPLATE RESORBABLE BONE SCREW
| Applicant | Bioplate, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Nov 28, 2001 |
| Received | Aug 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012908
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.