RELIMESH


Device Classification Name

mesh, surgical, polymeric

510(k) Number K081327
Device Name RELIMESH
Applicant
HERNIAMESH S.R.L.
8 orange dr.
jericho, 
NY 
11753

Applicant Contact lorena trabucco
Correspondent
HERNIAMESH S.R.L.
8 orange dr.
jericho, 
NY 
11753

Correspodent Contact lorena trabucco
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 05/12/2008
Decision Date 06/19/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No