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RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K991784
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1999
Days to Decision
30 days
Submission Type
Summary

RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K991784
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1999
Days to Decision
30 days
Submission Type
Summary