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FDA 510(k)

Invictus Robotic Navigation Instruments

K-Number: K232044 · 2023-10-06

Decision Date2023-10-06
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Invictus Robotic Navigation Instruments is a medical device manufactured by Alphatec Spine, Inc.. It received FDA 510(k) clearance on 2023-10-06 under approval number K232044. 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 Invictus Robotic Navigation Instruments?

Invictus Robotic Navigation Instruments is a medical device that received FDA 510(k) clearance on 2023-10-06. It is manufactured by Alphatec Spine, Inc.. The 510(k) number is K232044.

When was Invictus Robotic Navigation Instruments approved by the FDA?

Invictus Robotic Navigation Instruments received FDA 510(k) clearance on 2023-10-06, under approval number K232044.

What company makes Invictus Robotic Navigation Instruments?

Invictus Robotic Navigation Instruments is manufactured by Alphatec Spine, Inc..

What is the FDA product code for Invictus Robotic Navigation Instruments?

The FDA product code for Invictus Robotic Navigation Instruments is OLO.

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Official Source

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