Last synced on 14 November 2025 at 11:06 pm

MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

Page Type
Cleared 510(K)
510(k) Number
K071300
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2007
Days to Decision
72 days
Submission Type
Summary

MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

Page Type
Cleared 510(K)
510(k) Number
K071300
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2007
Days to Decision
72 days
Submission Type
Summary