510(k) K170890 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TELIX K Interbody System
| Applicant | Biedermann Motech GmbH & Co. KG, Villingen-Schwenningen, DE |
| Decision | Substantially Equivalent, Jun 2, 2017 |
| Received | Mar 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170890
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.