The following data is part of a premarket notification filed by Vascutek Ltd. with the FDA for Gelseal Vascular Grafts, Gelsoft Vascular Grafts, Gelsoft Plus Vascular Grafts.
Device ID | K162803 |
510k Number | K162803 |
Device Name: | Gelseal Vascular Grafts, Gelsoft Vascular Grafts, Gelsoft Plus Vascular Grafts |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | VASCUTEK LTD. NEWMAINS AVE, Inchinnan, GB Pa4 9rr |
Contact | Neil Mclachlan |
Correspondent | Neil Mclachlan VASCUTEK LTD. NEWMAINS AVE, Inchinnan, 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 | 2016-10-05 |
Decision Date | 2017-07-14 |
Summary: | summary |