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PROSTIVA RF THERAPY HAND PIECE, MODEL 8929

Page Type
Cleared 510(K)
510(k) Number
K082464
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2008
Days to Decision
61 days
Submission Type
Summary

PROSTIVA RF THERAPY HAND PIECE, MODEL 8929

Page Type
Cleared 510(K)
510(k) Number
K082464
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2008
Days to Decision
61 days
Submission Type
Summary