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LAMITRODE LEADS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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