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ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053250
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2005
Days to Decision
24 days
Submission Type
Statement

ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053250
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2005
Days to Decision
24 days
Submission Type
Statement