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NervAlign Nerve Cuff

Page Type
Cleared 510(K)
510(k) Number
K202234
510(k) Type
Traditional
Applicant
Renerve Ltd
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
2/10/2022
Days to Decision
552 days
Submission Type
Summary

NervAlign Nerve Cuff

Page Type
Cleared 510(K)
510(k) Number
K202234
510(k) Type
Traditional
Applicant
Renerve Ltd
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
2/10/2022
Days to Decision
552 days
Submission Type
Summary