Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K152566 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor. | 2 | 11/29/2024 | Smith & Nephew Inc. |
TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure att... | 2 | 02/19/2020 | Smith & Nephew, Inc. |
-