510(k) K992158 ยท JEY Plate, Bone
LACTOSORB SHEETS
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 20, 1999 |
| Received | Jun 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992158
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.