CORUS Spinal System
K-Number: K190201 · 2019-03-08
ApplicantProvidence Medical Technology, Inc.
Decision Date2019-03-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CORUS Spinal System is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2019-03-08 under approval number K190201. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CORUS Spinal System?
CORUS Spinal System is a medical device that received FDA 510(k) clearance on 2019-03-08. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K190201.
When was CORUS Spinal System approved by the FDA?
CORUS Spinal System received FDA 510(k) clearance on 2019-03-08, under approval number K190201.
What company makes CORUS Spinal System?
CORUS Spinal System is manufactured by Providence Medical Technology, Inc..
What is the FDA product code for CORUS Spinal System?
The FDA product code for CORUS Spinal System is HRX.
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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.