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 |