FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

Attain Select II + SureValve delivery catheter system, Attain Command + SureValve Left Heart Delivery System, Attain Comman + SureValve Guide Catheters for Left Heart Delivery, C315 Delivery Catheter

K Number: K192712 · Decision Aug 3, 2020
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
209
Review Days
311

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Basic Information

Device Name
Attain Select II + SureValve delivery catheter system, Attain Command + SureValve Left Heart Delivery System, Attain Comman + SureValve Guide Catheters for Left Heart Delivery, C315 Delivery Catheter
K Number
K192712
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Inc.
Date Received
September 27, 2019
Decision Date
August 3, 2020
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

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K251831 Bio-Medicus Life Support Catheter and Introducer
K253511 Concerto Versa™ Detachable Coil
K253409 C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48)
K251258 MC2™ Two-Stage Venous Cannula; MC2X™ Three-Stage Venous Cannula
K250075 Medtronic Stedi Extra Support Guidewire
K250199 VitalFlow Console
K250558 SelectSite C304 Deflectable Catheter System (C304); C315 Delivery System (C315)
Search all 209 clearances from Medtronic, Inc. →