Retention Device, Suture
Arthrex, Inc.'s record for this product code
MDR events37All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
37 adverse event reports on file
- ARTHREXJan 6, 2011InjuryMW5018920
- PEEK CORKSCREW FT W/ NEEDLES, 4.5MMJul 17, 2008Injury1220246-2008-00135
- PEEK CORKSCREW FT W/ NEEDLES, 4.5MMJul 17, 2008Injury1220246-2008-00136
- PUSHLOCK, PEEK, 3.5MM X 14MMJul 14, 2008Other1220246-2008-00129
- SUTURE BUTTON 3.5MM, STERILEFeb 29, 2008Other1220246-2008-00026
- CORKSCREW II SUTURE ANCHOR, 5X15MMNov 14, 2007Injury1220246-2007-00246
- CORKSCREW II SUTURE ANCHOR, 5X15MMNov 14, 2007Injury1220246-2007-00248
- BIO-PUSHLOCK 3.5MM X 14MMSep 21, 2007Other1220246-2007-00196
- BIO-FASTAK SUTURE ANCHOR WITH #2 FIBERWIREJun 28, 2007Other1220246-2007-00117
- CORKSCREW FT 11 SUTURE ANCHOR W/2 FIBURWIREApr 17, 2007MalfunctionMW1042634
Recalls
0 recall events for this product code
No recalls on file for Arthrex, Inc. under 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.