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Arthrotek/Biomet, Inc.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K981967 WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCREMBI1998-07-17 View
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