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PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K113380
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2012
Days to Decision
365 days
Submission Type
Summary

PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K113380
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2012
Days to Decision
365 days
Submission Type
Summary