Last synced on 20 December 2024 at 11:05 pm

ANS AXXESS PERCUTANEOUS LEAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032034
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2003
Days to Decision
94 days
Submission Type
Statement

ANS AXXESS PERCUTANEOUS LEAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032034
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2003
Days to Decision
94 days
Submission Type
Statement