Last synced on 27 December 2024 at 11:04 pm

Rebuilder Nerve Guidance Conduit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230794
510(k) Type
Traditional
Applicant
CelestRay Biotech Company, LLC.,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2024
Days to Decision
313 days
Submission Type
Summary

Rebuilder Nerve Guidance Conduit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230794
510(k) Type
Traditional
Applicant
CelestRay Biotech Company, LLC.,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2024
Days to Decision
313 days
Submission Type
Summary