CAVUX CervicalCage-L SA System
K-Number: K163474 · 2017-03-10
ApplicantProvidence Medical Technology, Inc.
Decision Date2017-03-10
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CAVUX CervicalCage-L SA System is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2017-03-10 under approval number K163474. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CAVUX CervicalCage-L SA System?
CAVUX CervicalCage-L SA System is a medical device that received FDA 510(k) clearance on 2017-03-10. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K163474.
When was CAVUX CervicalCage-L SA System approved by the FDA?
CAVUX CervicalCage-L SA System received FDA 510(k) clearance on 2017-03-10, under approval number K163474.
What company makes CAVUX CervicalCage-L SA System?
CAVUX CervicalCage-L SA System is manufactured by Providence Medical Technology, Inc..
What is the FDA product code for CAVUX CervicalCage-L SA System?
The FDA product code for CAVUX CervicalCage-L SA System is OVE.
Other Devices by Providence Medical Technology, Inc.
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K161442NuVasive® CoRoent® Small Interlock SystemNu Vasive, Incorporated
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K160066Pro-Link® Stand-Alone Cervical Spacer SystemLife Spine, Inc.
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.