510(k) K023237

XYLOS SURGICAL MESH by Xylos Corporation — Product Code FTM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 2003
Date Received
September 27, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical
Device Class
Class II
Regulation Number
878.3300
Review Panel
SU
Submission Type