510(k) K952168 ยท JEY Plate, Bone
TITANIUM MANDIBULAR FRACTURE SYSTEM
| Applicant | Medicon, Inc., D-78532/Tuttlingen, DE |
| Decision | Substantially Equivalent, Jun 22, 1995 |
| Received | May 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952168
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.