The following data is part of a premarket notification filed by Sulzer Medica with the FDA for Sulzer Vascutek Sealptfe Vascular Prosthesis.
Device ID | K993667 |
510k Number | K993667 |
Device Name: | SULZER VASCUTEK SEALPTFE VASCULAR PROSTHESIS |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | SULZER MEDICA 1300 EAST ANDERSON LN. Austin, TX 78752 -1793 |
Contact | Edward E Newton |
Correspondent | Edward E Newton SULZER MEDICA 1300 EAST ANDERSON LN. Austin, TX 78752 -1793 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-11-01 |
Decision Date | 2000-01-28 |
Summary: | summary |