510(k) K920116 ยท KWP Appliance, Fixation, Spinal Interlaminal
PWB LUMBOSACRAL SPINE SYSTEM
| Applicant | Cross Medical Products, Inc., Concord CA, US |
| Decision | Substantially Equivalent for Some Indications, Apr 10, 1992 |
| Received | Jan 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920116
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.