510(k) K800142 ยท JDS Nail, Fixation, Bone
FUSON BONE PLUG, RADIOPAQUE
| Applicant | Zimmer, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 19, 1980 |
| Received | Jan 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800142
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.