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LAMITRODE S-SERIES (S4 AND S8) LEADS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022222
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEM,INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2002
Days to Decision
30 days
Submission Type
Statement

LAMITRODE S-SERIES (S4 AND S8) LEADS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022222
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEM,INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2002
Days to Decision
30 days
Submission Type
Statement