RADIUS SNARE


Device Classification Name

device, percutaneous retrieval

510(k) Number K021441
Device Name RADIUS SNARE
Original Applicant
RADIUS MEDICAL TECHNOLOGIES, INC.
63 great rd.
maynard, 
MA 
01754

Original Contact maureen finlayson
Regulation Number 870.5150
Classification Product Code
MMX  
Date Received 05/06/2002
Decision Date 06/14/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No