510(k) K936269 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CASPAR TITANIUM ALLOY BONE SCREWS
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent for Some Indications, Aug 15, 1994 |
| Received | Dec 30, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936269
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.