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GFX NERVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063753
510(k) Type
Traditional
Applicant
ACI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2007
Days to Decision
183 days
Submission Type
Summary

GFX NERVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063753
510(k) Type
Traditional
Applicant
ACI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2007
Days to Decision
183 days
Submission Type
Summary