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A127 LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K030461
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2003
Days to Decision
71 days
Submission Type
Statement

A127 LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K030461
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2003
Days to Decision
71 days
Submission Type
Statement