510(k) K894283 ยท KQX Goniometer, Ac-Powered
COMPREHENSIVE SPINE MOTION ANALYZER
| Applicant | Orthopedic Systems, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Jan 19, 1990 |
| Received | Jun 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894283
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.