510(k) K001231 ยท HWC Screw, Fixation, Bone
THE KALIX IMPLANT
| Applicant | New Deal, S.A., Potomac MD, US |
| Decision | Substantially Equivalent, Jul 11, 2000 |
| Received | Apr 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001231
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.