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MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051773
510(k) Type
Special
Applicant
Medtronic Inc.,Neurological Division.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2005
Days to Decision
27 days
Submission Type
Summary

MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051773
510(k) Type
Special
Applicant
Medtronic Inc.,Neurological Division.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2005
Days to Decision
27 days
Submission Type
Summary