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

Attain Command + SureValve Delivery System, Attain Select II + SureValve delivery system

K Number: K222873 · Decision Nov 7, 2022
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
33
Review Days
46

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Basic Information

Device Name
Attain Command + SureValve Delivery System, Attain Select II + SureValve delivery system
K Number
K222873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic
Date Received
September 22, 2022
Decision Date
November 7, 2022
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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