510(k) K170243 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LOSPA IS TLIF & DLIF Cages
| Applicant | Corentec Co., Ltd., Cheonan, KR |
| Decision | Substantially Equivalent, Mar 31, 2017 |
| Received | Jan 26, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170243
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.