Arthrex, Inc.HTWClass I

Bit, Drill

Arthrex, Inc.'s record for this product code

MDR events391All time

Recalls1All time

510(k) clearances0All time

Recent MDR events

391 adverse event reports on file

Recalls

1 recall events for this product code

TerminatedUnknown
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
View FDA record ↗

510(k) clearances

0 clearances for this product code

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