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

ATTAIN 6227DEF DEFLECTABLE CATHETER DELIVERY SYSTEM

K Number: K061480 · Decision Aug 21, 2006
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
7
Review Days
83

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
ATTAIN 6227DEF DEFLECTABLE CATHETER DELIVERY SYSTEM
K Number
K061480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Ireland
Date Received
May 30, 2006
Decision Date
August 21, 2006
Product Code
DQY
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
DQY Catheter, Percutaneous

Similar 510(k) Clearances

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

View all

Other Clearances by Medtronic, Ireland

K Number Device Name
K251970 Sprinter Legend Rapid Exchange Balloon Dilatation Catheter
K252390 Telescope Guide Extension Catheter
K250787 Liberant Thrombectomy System
K123153 ATTAIN COMMAND+SUREVALVE LEFT HEART DELIVERY SYSTEM ATTAIN COMMAND GUIDE CATHETERS FOR LEFT HEART DELIVERY,ATTAIN SELECT
K103095 SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON
K053431 ATTAIN SELECT II 6248DEL DELIVERY CATHETER SYSTEM