FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Traxcess 7 Mini Guidewire

K Number: K201487 · Decision Jul 2, 2020
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
39
Applicant Total
85
Review Days
28

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Traxcess 7 Mini Guidewire
K Number
K201487
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MicroVention, Inc.
Date Received
June 4, 2020
Decision Date
July 2, 2020
Product Code
MOF
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOF Guide, Wire, Catheter, Neurovasculature

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOF), ordered by most recent decision date.

View all

Other Clearances by MicroVention, Inc.

K Number Device Name
K232542 Wedge XL Delivery Catheter
K230775 SOFIA EX Intracranial Support Catheter
K222694 EmPro EPS (EP4514C-190, EP6514C-190);Nanoparasol EPS (PNP4514C-190,PNP6514C-190)
K222115 ISAAC Neurovascular Navigation Catheter
K223050 AZUR HydroPack 18 (45-880005; 45-880010; 45-880020; 45-880035; 45-880050; 45-880060)
K214024 SOFIA 88 Catheter
K211120 ERIC Retrieval Device
K193607 BOBBY Balloon Guide Catheter
K200547 Traxcess 14 SELECT Guidewire
K191680 AZUR Vascular Plug
Search all 85 clearances from MicroVention, Inc. →