Medical Device Recalls
-
11 to 14 of 14 Results
510(K) Number: K002757 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Biomet OSS Letson Proximal Femoral Trial 7 cm resection/right, stainless steel, Biomet Orthopedics, ... | 2 | 06/29/2009 | Biomet, Inc. |
Biomet OSS Interlok IM Stem w/Screw, straight collar, 13 mm x 225 mm, TI6AL4V alloy, sterile, Biomet... | 2 | 09/11/2008 | Biomet, Inc. |
Biomet OSS Interlok IM Stem w/Screw, straight collar, 15 mm x 225 mm, TI6AL4V alloy, sterile, Biomet... | 2 | 09/11/2008 | Biomet, Inc. |
Biomet OSS Interlok IM Stem w/Screw, straight collar, 11 mm x 225 mm, TI6AL4V alloy, sterile, Biomet... | 2 | 09/11/2008 | Biomet, Inc. |
-