510(k) K130274 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BIOLIGN ACIF SYSTEMS, BIOLIGN STACC ACIF SYSTEM, BIOLIGN TLIF SYSTEM
| Applicant | Elite Surgical Supplies (Pty), Ltd., Pretoria West Industrial, ZA |
| Decision | Substantially Equivalent, Oct 29, 2013 |
| Received | Feb 4, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130274
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.