Radius Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radius Medical Technologies, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Radius Medical Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in Hopkonton, US.
Historical record: 9 cleared submissions from 1997 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Radius Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Radius Medical Technologies, Inc.
9 devices
Cleared
Oct 04, 2007
RADIUS SNARE
Cardiovascular
225d
Cleared
Sep 25, 2007
MODIFICATION TO RADIUS SNARE
Cardiovascular
123d
Cleared
Oct 17, 2003
RADIUS COUGAR WIRE
Cardiovascular
30d
Cleared
Jul 17, 2003
RADIUS 018 COUGAR WIRE
Cardiovascular
7d
Cleared
Feb 03, 2003
RADIUS MICRO SNARE
Cardiovascular
213d
Cleared
Jun 14, 2002
RADIUS SNARE
Cardiovascular
39d
Cleared
Aug 23, 2001
RADIUS NEXT GENERATION GUIDEWIRE
Gastroenterology & Urology
78d
Cleared
May 25, 2001
RADIUS COUGAR WIRE
Cardiovascular
28d
Cleared
May 20, 1997
RADIUS PTCA GUIDEWIRE
Cardiovascular
102d