CORUS-LX Implant
K-Number: K253190 · 2025-11-20
ApplicantProvidence Medical Technology, Inc.
Decision Date2025-11-20
Product CodeMRW
DecisionSubstantially Equivalent
Device Summary
CORUS-LX Implant is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2025-11-20 under approval number K253190. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CORUS-LX Implant?
CORUS-LX Implant is a medical device that received FDA 510(k) clearance on 2025-11-20. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K253190.
When was CORUS-LX Implant approved by the FDA?
CORUS-LX Implant received FDA 510(k) clearance on 2025-11-20, under approval number K253190.
What company makes CORUS-LX Implant?
CORUS-LX Implant is manufactured by Providence Medical Technology, Inc..
What is the FDA product code for CORUS-LX Implant?
The FDA product code for CORUS-LX Implant is MRW.
Other Devices by Providence Medical Technology, Inc.
Related Devices (Code: MRW)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.