510(k) K992012 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
WILTSE SYSTEM
| Applicant | Advanced Spine Fixation Systems, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 4, 2000 |
| Received | Jun 15, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992012
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.