XYLOS SURGICAL MESH


Device Classification Name

mesh, surgical

510(k) Number K023237
Device Name XYLOS SURGICAL MESH
Original Applicant
XYLOS CORPORATION
815 connecticut ave., nw.
suite 800
washington, 
DC 
20006

Original Contact patsy trisler
Regulation Number 878.3300
Classification Product Code
FTM  
Date Received 09/27/2002
Decision Date 03/18/2003
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