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FINESSE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072261
510(k) Type
Traditional
Applicant
Primaeva Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/2007
Days to Decision
134 days
Submission Type
Summary

FINESSE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072261
510(k) Type
Traditional
Applicant
Primaeva Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/2007
Days to Decision
134 days
Submission Type
Summary