inforMED
Arthrex, Inc.PLFClass II

Bone Wedge

Arthrex, Inc.'s record for this product code

MDR events3All time
Recalls6All time
510(k) clearances0All time

Recent MDR events

3 adverse event reports on file

Recalls

6 recall events for this product code

510(k) clearances

0 clearances for this product code

No 510(k) clearances on file for Arthrex, Inc. under this product code.