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MEDTRONIC DUAL CHANNEL SPINAL CORD STIM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812155
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1981
Days to Decision
71 days

MEDTRONIC DUAL CHANNEL SPINAL CORD STIM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812155
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1981
Days to Decision
71 days