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

SJM ATTUNE ANNULOPLASTY RING

K Number: K092876 · Decision Oct 16, 2009
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
74
Applicant Total
105
Review Days
28

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Basic Information

Device Name
SJM ATTUNE ANNULOPLASTY RING
K Number
K092876
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.3800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
St Jude Medical
Date Received
September 18, 2009
Decision Date
October 16, 2009
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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