K-number	K222220
Device name	SpinMedix Absorbable Fibrous Membrane
Applicant	Celestray Biotech Company, LLC.,
Product code	OWW
Device class	Class II
Decision date	Jul 6, 2023
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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SpinMedix Absorbable Fibrous Membrane

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