510(k) K102402 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SOLUS ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SPINAL SPACER SYSTEM
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Mar 30, 2011 |
| Received | Aug 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102402
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 29, 2012 | Alphatec Spine, Inc. SOLUS Anterior Lumbar Interbody Fusion Spinal
Spacer System, Solus Proximal/Distal Deployment Wrenches, 510(k) K102402.
The Alphatec Solus Anterior Lumbar Interbody Fusion (AUF) System is indicated f Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.