The following data is part of a premarket notification filed by Vascutek Ltd. with the FDA for Vascutek Branched Gelweave.
Device ID | K090987 |
510k Number | K090987 |
Device Name: | VASCUTEK BRANCHED GELWEAVE |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | VASCUTEK LTD. NEWMAINS AVE. Inchinnan, Renfrewshire, GB Pa4 9rr |
Contact | Karen Kelso |
Correspondent | Karen Kelso VASCUTEK LTD. NEWMAINS AVE. Inchinnan, Renfrewshire, GB Pa4 9rr |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-04-07 |
Decision Date | 2009-06-19 |
Summary: | summary |