510(k) K992441

ADVANTA GRAFT by Atrium Medical Corp. — Product Code DYF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 20, 1999
Date Received
July 22, 1999
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
Device Class
Class II
Regulation Number
870.3450
Review Panel
CV
Submission Type