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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