510(k) K131612 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ANYPLUS; ALIF PEEK CAGES, PLIF PEEK CAGES, T-PLIF PEEK CAGES, TLIF PEEK CAGES
| Applicant | GS Medical Co., Ltd., Douglassville PA, US |
| Decision | Substantially Equivalent, Apr 18, 2014 |
| Received | Jun 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131612
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.