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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 50 Results
ProductCode: JWH Applicant: Biomet, Inc Decision Date To: 12/05/2022
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Device Name
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510(K)
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agc v2 revision knee system BIOMET, INC. K984054 07/30/1999
ascent system BIOMET, INC. K982869 09/22/1998
maxim removable molded poly tibia BIOMET, INC. K984623 03/05/1999
titanium femoral component BIOMET, INC. K981996 03/10/1999
ascent knee system BIOMET, INC. K991428 05/21/1999
maxim knee system BIOMET, INC. K993159 10/14/1999
maxim removable molded poly tibia BIOMET, INC. K991753 08/17/1999
performance knee system BIOMET, INC. K992167 07/28/1999
anatomic total knee prosthesis BIOMET, INC. K000978 06/22/2000
ascent knee revision femoral stem BIOMET, INC. K001010 04/27/2000
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