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TELIGEN System Peripheral Motor Nerve Stimulation Indications

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223438
510(k) Type
Traditional
Applicant
Medos International, SARL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/10/2023
Days to Decision
88 days
Submission Type
Summary

TELIGEN System Peripheral Motor Nerve Stimulation Indications

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223438
510(k) Type
Traditional
Applicant
Medos International, SARL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/10/2023
Days to Decision
88 days
Submission Type
Summary