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

ENROUTE Transcarotid Neuroprotection System

K Number: K143072 · Decision Feb 9, 2015
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
35
Applicant Total
5
Review Days
105

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
ENROUTE Transcarotid Neuroprotection System
K Number
K143072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Silk Road Medical, Inc.
Date Received
October 27, 2014
Decision Date
February 9, 2015
Product Code
NTE
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
NTE Temporary Carotid Catheter For Embolic Capture

Similar 510(k) Clearances

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

View all

Other Clearances by Silk Road Medical, Inc.

K Number Device Name
K221414 ENROUTE Enflate Transcarotid RX Balloon Dilatation Catheter
K153485 ENROUTE Transcarotid Neuroprotection System
K143459 Silk Road Acccess Catheter
K130649 SILK ROAD ACCESS CATHETER