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EARP Nerve Cuff Electrode

Page Type
Cleared 510(K)
510(k) Number
K241917
510(k) Type
Special
Applicant
Retropsoas Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
30 days
Submission Type
Summary

EARP Nerve Cuff Electrode

Page Type
Cleared 510(K)
510(k) Number
K241917
510(k) Type
Special
Applicant
Retropsoas Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
30 days
Submission Type
Summary