ARTICOR planner
K-Number: K252195 · 2026-03-27
ApplicantArtiness S.R.L
Decision Date2026-03-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ARTICOR planner is a medical device manufactured by Artiness S.R.L. It received FDA 510(k) clearance on 2026-03-27 under approval number K252195. 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 ARTICOR planner?
ARTICOR planner is a medical device that received FDA 510(k) clearance on 2026-03-27. It is manufactured by Artiness S.R.L. The 510(k) number is K252195.
When was ARTICOR planner approved by the FDA?
ARTICOR planner received FDA 510(k) clearance on 2026-03-27, under approval number K252195.
What company makes ARTICOR planner?
ARTICOR planner is manufactured by Artiness S.R.L.
What is the FDA product code for ARTICOR planner?
The FDA product code for ARTICOR planner 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.