510(k) K041988 ยท JDR Staple, Fixation, Bone
ARTHROTEK MENISCAL HYBRID DEVICE
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 20, 2004 |
| Received | Jul 23, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041988
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.