510(k) K813581 ยท KGS Retention Device, Suture
CRUCIATE LIGAMENT BUTTON
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 23, 1982 |
| Received | Dec 28, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813581
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.