Last synced on 19 July 2024 at 11:05 pm

MODIFICATION TO RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032751
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
31 days
Submission Type
Statement

MODIFICATION TO RENEW LEAD EXTENSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032751
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
31 days
Submission Type
Statement