Medical Device Recalls
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1 result found
510(K) Number: K003281 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is i... | 2 | 05/07/2018 |
FEI # 1825034 Zimmer Biomet, Inc. |
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