510(k) K951846 ยท KWP Appliance, Fixation, Spinal Interlaminal
MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS
| Applicant | Alphatec Mfg., Inc., Concord CA, US |
| Decision | Substantially Equivalent for Some Indications, Feb 14, 1996 |
| Received | Apr 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951846
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.