FDA 510(k) Applications Submitted by Meenakshi Gupta

FDA 510(k) Number Submission Date Device Name Applicant
K200227 01/30/2020 Journey II XR Knee Instrument Smith & Nephew, Inc
K190730 03/21/2019 IODOSORB Smith & Nephew Medical Ltd.
K190756 03/25/2019 IODOFLEX Smith & Nephew Medical Ltd.
K191211 05/06/2019 JOURNEY II Unicompartmental Knee System Smith & Nephew, Inc.
K182109 08/03/2018 REDAPT Modular Acetabular Shell Smith & Nephew, Inc.
K182535 09/14/2018 R3 Anteverted Liners Smith & Nephew, Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact