K-number	K251720
Device name	OsteoFlo HydroFiber
Applicant	SurGenTec, LLC
Product code	MQV
Device class	Class II
Decision date	Jul 2, 2025
Decision	Substantially Equivalent
Regulation	888.3045

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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OsteoFlo HydroFiber

Everything you need for a 510(k) submission. Nothing you don't.