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VentriPoint Medical System

Page Type
Cleared 510(K)
510(k) Number
K150628
510(k) Type
Traditional
Applicant
VENTRIPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2015
Days to Decision
72 days
Submission Type
Summary

VentriPoint Medical System

Page Type
Cleared 510(K)
510(k) Number
K150628
510(k) Type
Traditional
Applicant
VENTRIPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2015
Days to Decision
72 days
Submission Type
Summary