Medical Device Recalls
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1 result found
510(K) Number: K093670 |
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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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Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows fo... | 1 | 08/22/2013 | Stryker Spine |
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