Blueprint Mixed Reality system
K-Number: K222510 · 2023-01-20
ApplicantTornier S.A.S.
Decision Date2023-01-20
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Blueprint Mixed Reality system is a medical device manufactured by Tornier S.A.S.. It received FDA 510(k) clearance on 2023-01-20 under approval number K222510. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Blueprint Mixed Reality system?
Blueprint Mixed Reality system is a medical device that received FDA 510(k) clearance on 2023-01-20. It is manufactured by Tornier S.A.S.. The 510(k) number is K222510.
When was Blueprint Mixed Reality system approved by the FDA?
Blueprint Mixed Reality system received FDA 510(k) clearance on 2023-01-20, under approval number K222510.
What company makes Blueprint Mixed Reality system?
Blueprint Mixed Reality system is manufactured by Tornier S.A.S..
What is the FDA product code for Blueprint Mixed Reality system?
The FDA product code for Blueprint Mixed Reality system is OLO.
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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.