510(k) K141217 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACCULIF TL AND PL CAGE
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 16, 2014 |
| Received | May 12, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141217
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 26, 2016 | Howmedica Osteonics Corp. AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous Terminated |
MAX | None listed |
| Jul 26, 2016 | Howmedica Osteonics Corp. AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellou Terminated |
MAX | None listed |
| Jul 26, 2016 | Howmedica Osteonics Corp. AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancello Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.