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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K221545
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Product Description
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Recall
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FDA Recall
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MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device 2 04/19/2023 Medacta Usa Inc
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device 2 04/19/2023 Medacta Usa Inc
MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device 2 04/19/2023 Medacta Usa Inc
MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device 2 04/19/2023 Medacta Usa Inc
MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device 2 04/19/2023 Medacta Usa Inc
MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device 2 04/19/2023 Medacta Usa Inc
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