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 |