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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 7 of 7 Results
510(K) Number: K082078
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Product Description
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FDA Recall
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DIST LAT FEM LOCK PLT, LT 2 12/27/2013 Zimmer, Inc.
DIST LAT FEM LOCK PLT, RT 2 12/27/2013 Zimmer, Inc.
FEM COND BUTTRESS PLT, LT 2 12/27/2013 Zimmer, Inc.
FEM COND BUTTRESS PLT, RT. 2 12/27/2013 Zimmer, Inc.
ITST THREADED GUIDE PIN 2 12/27/2013 Zimmer, Inc.
Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 4723580... 2 11/07/2019 Zimmer Biomet, Inc.
ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM DISTAL MEDIAL HUMERAL LOCKING PLATE, SHORT RIGHT 11 H... 2 08/27/2013 Zimmer, Inc.
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