FDA 510(k) Applications Submitted by GARRY T. HAYECK
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K150753 |
03/23/2015 |
OASYS System |
STRYKER CORPORATION |
| K151726 |
06/26/2015 |
AVS AL and AVS ALign PEEK Spacers, AVS PL and AVS UniLIF PEEK Spacers, AVS TL PEEK Spacer, AVS Navigator PEEK Spacer, AVS ARIA PEEK Spacer |
Stryker Corporation |
| K151755 |
06/29/2015 |
OASYS(r) System |
Stryker Corporation |
| K142251 |
08/14/2014 |
AVS AS PEEK Spacer |
Stryker Corporation |
| K142381 |
08/26/2014 |
Xia 3 Spinal System |
STRYKER CORP. |
| K142741 |
09/24/2014 |
OASYS System |
STRYKER CORPORATION |
| K143163 |
11/03/2014 |
AVS« AL and ALign PEEK Spacers, AVS« PL and UniLIF PEEK Spacers, AVS« TL PEEK Spacer, AVS« Navigator PEEK Spacer, AVS« ARIA PEEK Spacer, AccuLIF TL and PL Cage, AVS« Anchor-L Spacer, Aero-AL Lumbar Cage System |
STRYKER CORPORATION |
| K142114 |
08/04/2014 |
Xia« Growth Rod Conversion Set |
STRYKER CORPORATION |
| K150449 |
02/20/2015 |
LITe Plate System |
STRYKER CORP. |
| K150539 |
03/03/2015 |
OASYS System |
Stryker Corporation |
| K160813 |
03/24/2016 |
EasyStep |
STRYKER GMBH |
| K153154 |
11/02/2015 |
Asnis JFX System |
Stryker Trauma AG |
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