Anatase Spine Surgery Navigation System
K-Number: K230783 · 2023-04-21
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
Other Devices by Remex Medical Corp.
Related Devices (Code: OLO)
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.