510(k) K970841 ยท JEY Plate, Bone
IMTEC/TITANIUM MESH
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Apr 30, 1997 |
| Received | Mar 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970841
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.