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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K102795
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Signature TKA GDE/MDL Set 04-05 Patient-specific surgical guide and instrument set. 2 06/09/2016 Materialise USA LLC
Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surg... 2 10/23/2015 Materialise N.V.
Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides ar... 2 03/17/2015 Materialise N.V.
REF 42-422561 SIGNATURE QTY, 1 TKA GDE/MDL (Prosthesis, knee) SET 04-05 DGHUMPHR-NOV52LKA-J_K-004320... 2 03/02/2012 Biomet, Inc.
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