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MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD

Page Type
Cleared 510(K)
510(k) Number
K030674
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
24 days
Submission Type
Statement

MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD

Page Type
Cleared 510(K)
510(k) Number
K030674
510(k) Type
Special
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
24 days
Submission Type
Statement