Orthoscan Tau Mini C-Arm
K-Number: K213113 · 2021-10-21
ApplicantOrthoscan, Inc.
Decision Date2021-10-21
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Orthoscan Tau Mini C-Arm is a medical device manufactured by Orthoscan, Inc.. It received FDA 510(k) clearance on 2021-10-21 under approval number K213113. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Orthoscan Tau Mini C-Arm?
Orthoscan Tau Mini C-Arm is a medical device that received FDA 510(k) clearance on 2021-10-21. It is manufactured by Orthoscan, Inc.. The 510(k) number is K213113.
When was Orthoscan Tau Mini C-Arm approved by the FDA?
Orthoscan Tau Mini C-Arm received FDA 510(k) clearance on 2021-10-21, under approval number K213113.
What company makes Orthoscan Tau Mini C-Arm?
Orthoscan Tau Mini C-Arm is manufactured by Orthoscan, Inc..
What is the FDA product code for Orthoscan Tau Mini C-Arm?
The FDA product code for Orthoscan Tau Mini C-Arm is OXO.
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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.