Monteris Medical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Monteris Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Winnipeg, Mb, CA.
Historical record: 8 cleared submissions from 2011 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Monteris Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Monteris Medical, Inc.
8 devices
Cleared
Aug 21, 2020
NeuroBlate System
Neurology
122d
Cleared
Jul 25, 2017
Monteris Medical NeuroBlate System
General & Plastic Surgery
88d
Cleared
Oct 26, 2016
NeuroBlate System
General & Plastic Surgery
26d
Cleared
Feb 19, 2015
NeuroBlate System
General & Plastic Surgery
78d
Cleared
Jul 30, 2013
NEUROBLATE(TM) SYSTEM
General & Plastic Surgery
33d
Cleared
Jul 11, 2013
MONTERIS MEDICAL NEUROBLATE SYSTEM
General & Plastic Surgery
66d
Cleared
Apr 01, 2013
NEUROBLATE SYSTEM
General & Plastic Surgery
402d
Cleared
Apr 08, 2011
ATAMA SYSTEM
Radiology
53d