Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K071174 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pathfinder End Screw Extender Sleeve, REF 1165-10, Rx, non-sterile, sold under label Abbott Spine, I... | 2 | 10/18/2010 | Zimmer Inc. |
Abbott Spine PathFinder, Cannulated Poly Screwdriver II - MOD, non-sterile, Manufactured by Abbott S... | 2 | 08/31/2010 | Zimmer Inc. |
PathFinder Cannulated T-Handle Bone Awl, Part Number 1155-2; distributed by Abbott Spine, Inc., Aust... | 2 | 09/05/2008 | Abbott Spine |
PathFinder® Spinal Fixation System T-Handle Driver; Part 2151-7 (13" shaft); Non-sterile, Reusable I... | 2 | 09/01/2008 | Abbott Spine |
-