Medical Device Recalls
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1 result found
510(K) Number: K932807 |
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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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| Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixa... | 2 | 12/08/2020 |
FEI # 3003418325 Integra LifeSciences Corp. |
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