510(k) K061783 ยท JDS Nail, Fixation, Bone
KNEE FUSION NAIL
| Applicant | Smith & Nephew, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Aug 10, 2006 |
| Received | Jun 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061783
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.