510(k) K983622 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
BODYFORM THORACO-LUMBAR FIXATION SYSTEM
| Applicant | Theken Surgical,Llc, Barberton OH, US |
| Decision | Substantially Equivalent, Dec 30, 1998 |
| Received | Oct 15, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983622
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.