510(k) K111122 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
AESCULAP SIBD XP SPINAL SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Aug 4, 2011 |
| Received | Apr 21, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111122
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.