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. |
|
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