510(k) K171425 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONCORDE LIFT
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Jul 20, 2017 |
| Received | May 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171425
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 27, 2019 | DePuy Spine, Inc. Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (US197809026C) Terminated |
MAX | None listed |
| Jul 26, 2017 | DePuy Orthopaedics, Inc. Concorde Lift Driver Shaft AO.
Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine. Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.