Medtronic Advanced Energy - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Medtronic Advanced Energy has 8 FDA 510(k) cleared medical devices. Based in Portsmouth, US.
Historical record: 8 cleared submissions from 2014 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medtronic Advanced Energy Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic Advanced Energy
8 devices
Cleared
Jul 26, 2019
Medtronic Total Hip Arthroplasty System
Orthopedic
255d
Cleared
Aug 02, 2018
PlasmaBlade X 3.0S, PlasmaBlade X 4.0
General & Plastic Surgery
83d
Cleared
Sep 07, 2017
Minimally Invasive Sealer (MIS) Flex, Minimally Invasive Sealer (MIS) Flex Mini
General & Plastic Surgery
212d
Cleared
Apr 13, 2017
PlasmaBlade T
General & Plastic Surgery
43d
Cleared
Mar 20, 2017
CoreCath 2.7S
General & Plastic Surgery
48d
Cleared
Jul 08, 2016
PlasmaBlade TnA Tonsil and Adenoid Dissection Device
General & Plastic Surgery
291d
Cleared
May 21, 2015
PlasmaBlade UPPP and Suction Coagulator
General & Plastic Surgery
104d
Cleared
Dec 31, 2014
AEx Generator
General & Plastic Surgery
57d