Rebuilder Nerve Guidance Conduit— 510(k) K230794
Substantially EquivalentCelestray Biotech Company, LLC.,
FDA 510(k) clearance K230794 for Rebuilder Nerve Guidance Conduit, Substantially Equivalent on 2024-01-29. Applicant: Celestray Biotech Company, LLC.,. Device class: 2.
Clearance details
- Applicant
- Celestray Biotech Company, LLC.,
- Product code
- Code JXI
- Device class
- Class 2
- Regulation
- 21 CFR 882.5275
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bethesda, MD, US
Recent devices under product code JXI
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