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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Tornier S.A.S.. It received FDA 510(k) clearance on 2023-01-20 under 510(k) 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. The listed applicant is Tornier S.A.S.. The 510(k) number is K222510.

When did Blueprint Mixed Reality system receive FDA 510(k) clearance?

Blueprint Mixed Reality system received FDA 510(k) clearance on 2023-01-20, under 510(k) number K222510.

Who is the listed applicant for Blueprint Mixed Reality system?

The FDA 510(k) record lists Tornier S.A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Blueprint Mixed Reality system?

The FDA product code for Blueprint Mixed Reality system is OLO.

Other records listing Tornier S.A.S. as applicant

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Related Devices (Code: 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.

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