Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170503 |
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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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EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autogr... | 2 | 07/01/2022 | DePuy Spine, Inc. |
EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autogr... | 2 | 07/01/2022 | DePuy Spine, Inc. |
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