K-number	K230794
Device name	Rebuilder Nerve Guidance Conduit
Applicant	Celestray Biotech Company, LLC.,
Product code	JXI
Device class	Class II
Decision date	Jan 29, 2024
Decision	Substantially Equivalent
Regulation	882.5275

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Source

View the full FDA submission: accessdata.fda.gov

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Rebuilder Nerve Guidance Conduit

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