510(k) K981070 ยท JEY Plate, Bone
20-HOLE ADAPTATION PLATE
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Mar 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981070
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.