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LAMITRODE LEADS

Page Type
Cleared 510(K)
510(k) Number
K990469
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1999
Days to Decision
107 days
Submission Type
Summary

LAMITRODE LEADS

Page Type
Cleared 510(K)
510(k) Number
K990469
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1999
Days to Decision
107 days
Submission Type
Summary