FDA 510(k) Applications Submitted by Laura Medlin
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K100325 |
02/04/2010 |
PERI-LOC LOCKING HOLE INSERTS AND CABLE ACCESSORIES |
SMITH & NEPHEW, INC. |
K150648 |
03/12/2015 |
Arthrex DX SwiveLock SL with Forket Eyelet 3.5 x 8.5mm, Arthrex DX SwiveLock Suture Anchor, 3.5 x 13.5mm |
ARTHREX, INC. |
K090926 |
04/02/2009 |
SMITH & NEPHEW RAIL SYSTEM |
SMITH & NEPHEW, INC. |
K151256 |
05/12/2015 |
Arthrex BioSync« Bone Wedge |
Arthex, Inc |
K141735 |
06/27/2014 |
ARTHREX ANKLE FUSION PLATING SYSTEM |
ARTHREX, INC. |
K143047 |
10/23/2014 |
Arthrex iBalance Patella Implant, Dome |
ARTHREX, INC. |
K143749 |
12/31/2014 |
Arthrex Distal Radius System |
Arthrex, Inc. |
|
|