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MODIFICATION TO RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K032751
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
31 days
Submission Type
Statement

MODIFICATION TO RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K032751
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
31 days
Submission Type
Statement