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FDA 510(k) Applications Submitted by KRISTI ASHTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180327
02/06/2018
Stryker iVAS 13g Bone Biopsy Kit
Stryker Corporation
K150582
03/09/2015
Vertaplex« High Viscosity (HV) Radiopaque Bone Cement
STRYKER CORPORATION
K181752
07/02/2018
Stryker iVAS Elite Inflatable Vertebral Augmentation System (Stryker iVAS Elite Balloon Catheter)
Stryker Corporation
K172116
07/13/2017
Stryker iVAS Elite Inflatable Vertebral Augmentation System (Stryker iVAS Elite Balloon Catheter)
Stryker Corporation
K202393
08/21/2020
SpineJack Expansion Kit
Stryker Corporation
K172558
08/24/2017
iVAS 8g Bone Biopsy Kit, iVAS 11g Bone Biopsy Kit, iVAS 10g Bone Biopsy Kit
Stryker Corporation
K192818
10/01/2019
Vertaplex HV High Viscosity Radiopaque Bone Cement; ES2 Augmentable Spinal System
Stryker Corporation
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