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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K193396
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PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45... 2 05/03/2024 FEI # 3007728266
SPINEART SA
PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft... 2 06/28/2021 FEI # 3007728266
SPINEART SA
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