Cube Navigator
K-Number: K240620 · 2024-03-25
ApplicantMedical Templates AG
Decision Date2024-03-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Cube Navigator is a medical device manufactured by Medical Templates AG. It received FDA 510(k) clearance on 2024-03-25 under approval number K240620. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Cube Navigator?
Cube Navigator is a medical device that received FDA 510(k) clearance on 2024-03-25. It is manufactured by Medical Templates AG. The 510(k) number is K240620.
When was Cube Navigator approved by the FDA?
Cube Navigator received FDA 510(k) clearance on 2024-03-25, under approval number K240620.
What company makes Cube Navigator?
Cube Navigator is manufactured by Medical Templates AG.
What is the FDA product code for Cube Navigator?
The FDA product code for Cube Navigator is LLZ.
Related Devices (Code: LLZ)
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.