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

TransForm McCarthy Mitral Annuloplasty Ring (TF)

K Number: K250859 · Decision Jul 25, 2025
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
74
Applicant Total
14
Review Days
126

Basic Information

Device Name
TransForm McCarthy Mitral Annuloplasty Ring (TF)
K Number
K250859
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genesee Biomedical, Inc.
Date Received
March 21, 2025
Decision Date
July 25, 2025
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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Other Clearances by Genesee Biomedical, Inc.

K Number Device Name
K252917 ATLAAS (Atraumatic Left Atrial Appendage System) (AD)
K232599 TransForm McCarthy Mitral Annuloplasty Ring (TF)
K230679 WellsForm Tricuspid Annuloplasty Band (WF)
K202253 TruForm Sievers Annuloplasty Ring
K190506 NeoForm Annuloplasty Ring
K161815 FlexForm Annuloplasty Ring and FlexForm Annuloplasty Band
K093903 ATS TRI-AD SEMI-FLEXIBLE TRICUSPID ANUULOPLASTY, MODEL 900SFC
K090428 ATS SIMULUS ADJUSTABLE FLEXIBLE ANNULOPLASTY, MODEL 735 AC
K083683 ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SC
K072655 ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SR
Search all 14 clearances from Genesee Biomedical, Inc. →