Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K915132 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 14... | 2 | 06/01/2018 | Zimmer Biomet, Inc. |
MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM ... | 3 | 06/11/2015 | Biomet, Inc. |
Biomet Interlok 75 MM fixed I-Beam Tibial Plate with locking bar CO-CR-MO/TI 6AL 4V ALLOY, REF 14122... | 2 | 04/28/2011 | Biomet, Inc. |
Biomet CC Cruciate Tibial Tray, 67 mm.; Product No. 141232, Biomet, Inc., Warsaw, IN 46581 | 2 | 01/31/2008 | Biomet, Inc. |
Biomet CC Cruciate Tibial Tray, 75 mm.; Product No. 141234, Biomet, Inc., Warsaw, IN 46581 | 2 | 01/31/2008 | Biomet, Inc. |
Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Produ... | 2 | 11/24/2007 | Biomet, Inc. |
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