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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K232097
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IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF S... 2 02/23/2024 FEI # 2027467
Alphatec Spine, Inc.
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