510(k) K953720 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AESCULAP CASPAR PLATE & SCREW SYSTEM FOR ANTERIOR CERVICAL FUSION
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent for Some Indications, Nov 2, 1995 |
| Received | Aug 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953720
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.