K-number	K253190
Device name	CORUS-LX Implant
Applicant	Providence Medical Technology, Inc.
Product code	MRW
Device class	Class U
Decision date	Nov 20, 2025
Decision	Substantially Equivalent
Regulation	—

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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CORUS-LX Implant

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