510(k) K972332 ยท GXN Plate, Cranioplasty, Preformed, Non-Alterable
AESCULAP CRANIOFIX TITANIUM CLAMP SYSTEM
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Jan 16, 1998 |
| Received | Jun 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972332
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.