510(k) K014153 ยท HWC Screw, Fixation, Bone
COAPT SYSTMES ENDOTINE DEVICE
| Applicant | Coapt Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Mar 15, 2002 |
| Received | Dec 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014153
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.