Lemaitre Vascular

FDA Filings

This page includes the latest FDA filings for Lemaitre Vascular. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K190882 LeMaitre Vascular	XenoSure Biologic Patch	2020-02-13
PMN K190267 LeMaitre Vascular	EZE SIT Valvulotome	2019-10-30
PMN K182916 LeMaitre Vascular	Pruitt F3 Carotid Shunt, 10 Fr, Pruitt F3 Carotid Shunt, 9 Fr, Pruitt F3 Carotid Shunt, 8 Fr	2018-11-16

Similar & Related FDA Registered Companies

• LEMAITRE VASCULAR, INC.
• LeMaitre Vascular, Inc.63 Second Avenueburlington, MA 01803 PMA NumberN16837 Supplement NumberS029 Date Received12/30/2022 Decision Date01/25/2023 Product Code LXA  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• LeMaitre Vascular, Inc.63 Second Avenueburlington, MA 01803 PMA NumberN16837 Supplement NumberS028 Date Received09/16/2022 Decision Date10/14/2022 Product Code LXA  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No