Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072672 |
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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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Sequoia final driver closure top retention, non-sterile, REF 3384-2, Zimmer Spine, Austin, Texas, T... | 2 | 06/29/2011 | Zimmer Inc. |
Sequoia Spinal System Surgical Kits; Pedicle screw spinal system; Non-sterile (kits intended to be s... | 2 | 07/23/2008 | Abbott Spine |
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