510(k) K980288 ยท KWP Appliance, Fixation, Spinal Interlaminal
SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM
| Applicant | Spine-Tech, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent for Some Indications, Jul 29, 1998 |
| Received | Jan 26, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980288
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.