510(k) K023922 ยท HWC Screw, Fixation, Bone
COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197
| Applicant | Coapt Systems, Inc., Santa Rosa CA, US |
| Decision | Substantially Equivalent, Dec 20, 2002 |
| Received | Nov 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023922
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.