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FDA 510(k)

Anatase Spine Surgery Navigation System

K-Number: K230783 · 2023-04-21

Decision Date2023-04-21
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Anatase Spine Surgery Navigation System is a medical device manufactured by Remex Medical Corp.. It received FDA 510(k) clearance on 2023-04-21 under approval number K230783. 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 Anatase Spine Surgery Navigation System?

Anatase Spine Surgery Navigation System is a medical device that received FDA 510(k) clearance on 2023-04-21. It is manufactured by Remex Medical Corp.. The 510(k) number is K230783.

When was Anatase Spine Surgery Navigation System approved by the FDA?

Anatase Spine Surgery Navigation System received FDA 510(k) clearance on 2023-04-21, under approval number K230783.

What company makes Anatase Spine Surgery Navigation System?

Anatase Spine Surgery Navigation System is manufactured by Remex Medical Corp..

What is the FDA product code for Anatase Spine Surgery Navigation System?

The FDA product code for Anatase Spine Surgery Navigation System is OLO.

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Official Source

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