510(k) K172020 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Arlington PLIF/TLIF Cage
| Applicant | Signature Orthopaedics Pty, Ltd., Lane Cove West, AU |
| Decision | Substantially Equivalent, Nov 29, 2017 |
| Received | Jul 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172020
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.