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NEUROMOD STIMULATOR MODEL 3723

Page Type
Cleared 510(K)
510(k) Number
K780186
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1978
Days to Decision
24 days

NEUROMOD STIMULATOR MODEL 3723

Page Type
Cleared 510(K)
510(k) Number
K780186
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1978
Days to Decision
24 days