510(k) K954770 ยท KWP Appliance, Fixation, Spinal Interlaminal
CENTRA-LINE GRAPPLE, VARIFIX SYSTEM
| Applicant | Advanced Spine Fixation Systems, Inc., Cypress CA, US |
| Decision | Substantially Equivalent, Jan 25, 1996 |
| Received | Oct 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954770
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.