FDA 510(k) Applications Submitted by Catherine Kilshaw
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120229 |
01/25/2012 |
ENVOY DISTAL ACCESS GUIDING CATHETER |
Codman & Shurtleff, Inc. |
| K171439 |
05/16/2017 |
EAGLE Plus Anterior Cervical Plate System, EAGLE Plus Micro Anterior Cervical Plate System, PULSE Anterior Cervical Plate System, SKYLINE Anterior Cervical Plate System, SLIM LOC Anterior Cervical Plate System, SWIFT Plus Anterior Cervical Plate System, U |
Medos International SARL |
| K142185 |
08/08/2014 |
EXPEDIUM VERSE SPINE SYSTEM |
DEPUY SPINE, INC. |
| K142587 |
09/15/2014 |
Vertical Expandable Prosthetic Titanium Rib |
Depuy Synthes Spine, Inc. |
| K112828 |
09/28/2011 |
REVIVE INTERMEDIATE CATHETER (REVIVE IC) |
Codman & Shurtleff, Inc. |
| K123425 |
11/07/2012 |
TWINFIX TI 3.5MM SUTURE ANCHOR WITH TWO ULTRABRAID SUTURE #2 WITH NEEDLES, SL |
SMITH & NEPHEW, INC. |
| K123579 |
11/19/2012 |
FOOTPRINT ULTRA PK4.5MM AND 5.5MM SUTURE ANCHOR, SL |
SMITH & NEPHEW, INC. |
|
|
