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PAJUNK MULTISTIM SENSOR NERVE STIMULATORS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061172
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2006
Days to Decision
173 days
Submission Type
Summary

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061172
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2006
Days to Decision
173 days
Submission Type
Summary