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 |