Medical Device Recalls
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1 result found
510(K) Number: K180078 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an in... | 2 | 09/17/2024 |
FEI # 3004719693 Innovasis, Inc |
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