510(k) K012910 ยท JEY Plate, Bone
THE BIOPLATE MANDIBLE FIXATION SYSTEM
| Applicant | Bioplate, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Nov 20, 2001 |
| Received | Aug 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012910
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.