The following data is part of a premarket notification filed by Vascutek Ltd. with the FDA for Gelweave Branched Vascular Grafts With Radiopaque Markers.
Device ID | K093817 |
510k Number | K093817 |
Device Name: | GELWEAVE BRANCHED VASCULAR GRAFTS WITH RADIOPAQUE MARKERS |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | VASCUTEK LTD. NEWMAINS AVE. INCHINNAN INDUSTRIAL ESTATE Renfrewshire, Glasgow, GB Pa4 9rr |
Contact | Karen Kelso |
Correspondent | Karen Kelso VASCUTEK LTD. NEWMAINS AVE. INCHINNAN INDUSTRIAL ESTATE Renfrewshire, Glasgow, GB Pa4 9rr |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-12-11 |
Decision Date | 2010-01-07 |