510(k) K100802 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 20, 2010 |
| Received | Mar 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100802
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.