Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K031729 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Triathlon Femoral Distal Fixation Peg; Catalog Number 5575-X-00; Manufactured by Stryker Howmedica O... | 2 | 02/11/2011 | Stryker Howmedica Osteonics Corp. |
Triathlon Total Knee System Primary Tibial Baseplate; Sterile, Made in Ireland. Howmedica Osteoni... | 2 | 08/31/2010 | Stryker Howmedica Osteonics Corp. |
Triathlon X3 UHMWPE Tibial Inserts and Patellar Components, multiple sizes, Stryker Orthopaedics, Ma... | 2 | 03/02/2010 | Stryker Howmedica Osteonics Corp. |
-