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

Tri-Ad 2.0 Adams Tricuspid Band

K Number: K181132 · Decision May 29, 2018
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
74
Applicant Total
33
Review Days
29

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Basic Information

Device Name
Tri-Ad 2.0 Adams Tricuspid Band
K Number
K181132
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.3800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic
Date Received
April 30, 2018
Decision Date
May 29, 2018
Product Code
KRH
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
KRH Ring, Annuloplasty

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