510(k) K123993 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SOLUS ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Mar 5, 2013 |
| Received | Dec 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123993
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.