510(k) K913730 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AESCULAP TITANIUM BONE PLATES
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Mar 12, 1992 |
| Received | Aug 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913730
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.