Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K013979 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine, SlimLine Hybrid, Corpect... | 2 | 12/17/2005 | Abbott Spine |
SC-AcuFix Thinline Low-Profile Anterior Cervical Plate System manufactured by Spinal Concepts, Inc.,... | 2 | 06/11/2005 | Spinal Concepts, Inc |
-