510(k) K130782

ACCUMESH DEPLOYMENT SYSTEM by Covidien, LLC — Product Code ORQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 2013
Date Received
March 21, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

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

Intended to be used to facilitate the delivery of soft tissue prosthetics during the laparoscopic repair of soft tissue defects (e.G. Hernia repair).