510(k) K970635 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TITANIUM SPINAL ROD SYSTEM
| Applicant | Smith & Nephew, Inc., Orthopaedic Div., Memphis TN, US |
| Decision | Substantially Equivalent, Aug 14, 1997 |
| Received | Feb 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970635
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.