510(k) K962377 ยท KQX Goniometer, Ac-Powered
3D-SPINE
| Applicant | Skill Technologies, Inc., Phoenix AZ, US |
| Decision | Substantially Equivalent, Sep 3, 1996 |
| Received | Jun 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962377
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.