Last synced on 23 September 2022 at 11:05 pm

NervAlign Nerve Cuff

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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