ATRIUM LITE MESH


definition

Device Classification Name

mesh, surgical, polymeric

510(k) Number K002093
Device Name ATRIUM LITE MESH
Original Applicant
ATRIUM MEDICAL CORP.
5 wentworth dr.
hudson, 
NH 
03051

Original Contact joseph p de paolo
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 07/11/2000
Decision Date 07/24/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Special
Reviewed by Third Party No

Combination Product

No