510(k) K061776 ยท JDR Staple, Fixation, Bone
ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE
| Applicant | Arthrotek, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 25, 2006 |
| Received | Jun 23, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061776
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.