Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K143616 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicate... | 2 | 09/12/2016 | Howmedica Osteonics Corp. |
AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indica... | 2 | 09/12/2016 | Howmedica Osteonics Corp. |
AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicat... | 2 | 09/12/2016 | Howmedica Osteonics Corp. |
AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device system that uses h... | 2 | 02/23/2016 | Stryker Spine |
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