MicroVention, Inc. FDA Approvals

0 new drug approvals and 7 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Wedge XL Delivery Catheter510(k)May 16, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	May 16, 2024
SOFIA EX Intracranial Support Catheter510(k)Sep 14, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Sep 14, 2023
EmPro EPS (EP4514C-190, EP6514C-190);Nanoparasol EPS (PNP4514C-190,PNP6514C-190)510(k)Apr 27, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Apr 27, 2023
ISAAC Neurovascular Navigation Catheter510(k)Jan 10, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jan 10, 2023
AZUR HydroPack 18 (45-880005; 45-880010; 45-880020; 45-880035; 45-880050; 45-880060)510(k)Dec 21, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Dec 21, 2022
SOFIA 88 Catheter510(k)Sep 12, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Sep 12, 2022
ERIC Retrieval Device510(k)Mar 31, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Mar 31, 2022