Voyager Trajectory Array Guide (V-TAG)
K-Number: K191400 · 2019-06-21
ApplicantMri Interventions, Inc.
Decision Date2019-06-21
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Voyager Trajectory Array Guide (V-TAG) is a medical device manufactured by Mri Interventions, Inc.. It received FDA 510(k) clearance on 2019-06-21 under approval number K191400. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Voyager Trajectory Array Guide (V-TAG)?
Voyager Trajectory Array Guide (V-TAG) is a medical device that received FDA 510(k) clearance on 2019-06-21. It is manufactured by Mri Interventions, Inc.. The 510(k) number is K191400.
When was Voyager Trajectory Array Guide (V-TAG) approved by the FDA?
Voyager Trajectory Array Guide (V-TAG) received FDA 510(k) clearance on 2019-06-21, under approval number K191400.
What company makes Voyager Trajectory Array Guide (V-TAG)?
Voyager Trajectory Array Guide (V-TAG) is manufactured by Mri Interventions, Inc..
What is the FDA product code for Voyager Trajectory Array Guide (V-TAG)?
The FDA product code for Voyager Trajectory Array Guide (V-TAG) is HAW.
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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.