510(k) K980121 ยท KWP Appliance, Fixation, Spinal Interlaminal
AESCULAP SPINE SYSTEM ADDITIONAL COMPONENTS
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Jun 10, 1998 |
| Received | Jan 14, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980121
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.