The following data is part of a premarket notification filed by Vascutek Ltd. with the FDA for Modification To Eptfe Graft.
| Device ID | K041528 |
| 510k Number | K041528 |
| Device Name: | MODIFICATION TO EPTFE GRAFT |
| Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
| Applicant | VASCUTEK LTD. 6200 JACKSON RD. Ann Arbor, MI 48103 -9300 |
| Contact | Steven Arick |
| Correspondent | Steven Arick VASCUTEK LTD. 6200 JACKSON RD. Ann Arbor, MI 48103 -9300 |
| Product Code | DSY |
| CFR Regulation Number | 870.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-08 |
| Decision Date | 2004-09-14 |