FDA 510(k) Applications Submitted by SCOTT M DURLACHER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960516 |
02/05/1996 |
FASTAK SUTURE ANCHOR |
ARTHREX, INC. |
| K130810 |
03/25/2013 |
ZIMMER MOTIONLOC SCREW FOR PERIARTICULAR LOCKING PLATE SYSTEM |
ZIMMER, INC. |
| K981187 |
04/02/1998 |
ACL AVULSION LAG SCREW WITH SHEATH MODEL NUMBER AR-6001 |
ARTHREX, INC. |
| K971723 |
05/09/1997 |
FASTAK SUTURE ANCHOR (11.7MM)/(7.5MM) |
ARTHREX, INC. |
| K973812 |
10/07/1997 |
ARTHREX PUDDU OSTEOTOMY SYSTEM |
ARTHREX, INC. |
| K983577 |
10/13/1998 |
ARTHREX MENISCAL DART SYSTEM |
ARTHREX, INC. |
| K983843 |
10/30/1998 |
BIO-BUTTON 6.5MM, BIO-BUTTON 8MM, MODEL #'S AR-2236B & AR-2238B |
ARTHREX, INC. |
| K974847 |
12/29/1997 |
5.0MM PARACHUTE CORKSCREW SUTURE ANCHOR MODEL AR-22255, 3.5MM PARACHUTE CORKSCREW SUTURE ANCHOR MODEL AR-22235 |
ARTHREX, INC. |
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