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FDA 510(k) Applications Submitted by JONATHAN SCHELL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170725
03/09/2017
Stryker Universal Mesh
Stryker
K210861
03/23/2021
ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)
Stryker GmbH
K171152
04/20/2017
Stryker Universal Neuro III System AXS Screw
Stryker
K221346
05/09/2022
Stryker VariAx 2 MIS Calcaneus
Stryker GmbH
K151387
05/26/2015
Stryker Universal Neuro III System: UN III AXS Screw, UN III AXS Screwdriver Blade
STRYKER
K141633
06/18/2014
PRO-PICC WITH VALVE TECHNOLOGY
MEDICAL COMPONENTS INC
K161821
07/01/2016
Stryker Universal Mesh
Stryker
K152076
07/27/2015
PEEK Customized Cranial Implant, PEEK Customized Cranial Implant Priority
Stryker
K202289
08/12/2020
ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)
Stryker GmbH
K172572
08/28/2017
Stryker Upper-Face AXS screws and Mid-Face AXS screws
Stryker
K153248
11/09/2015
PEEK Customized Cranial Implant
STRYKER
K153508
12/07/2015
Stryker CMF MEDPOR Customized Implant
Stryker
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