510(k) K920256 ยท KQX Goniometer, Ac-Powered
SPINE MOTION ANALYZER WITH EMG
| Applicant | Orthopedic Systems, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Aug 10, 1992 |
| Received | Jan 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920256
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.