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FDA 510(k) Applications Submitted by Paul Nelson
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200398
02/18/2020
AxSOS 3 AF System and AxSOS 3 Ti System
Stryker GmbH
K180500
02/26/2018
VariAx 2 System
Stryker GmbH
K170771
03/14/2017
VariAx 2 Foot System
Stryker GmbH
K161753
06/24/2016
Hoffman LRF System
STRYKER GMBH
K173135
09/29/2017
VariAx 2 System
Stryker GmbH
K153377
11/23/2015
Hoffmann LRF (Limb Reconstruction Frame) System
Stryker GmbH
K163656
12/23/2016
Hoffmann LRF System
Stryker GmbH
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