Ankyras
K-Number: K230006 · 2023-12-28
ApplicantMentice Spain S.L.
Decision Date2023-12-28
Product CodePZO
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Ankyras is a medical device manufactured by Mentice Spain S.L.. It received FDA 510(k) clearance on 2023-12-28 under approval number K230006. The device is classified under product code PZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ankyras?
Ankyras is a medical device that received FDA 510(k) clearance on 2023-12-28. It is manufactured by Mentice Spain S.L.. The 510(k) number is K230006.
When was Ankyras approved by the FDA?
Ankyras received FDA 510(k) clearance on 2023-12-28, under approval number K230006.
What company makes Ankyras?
Ankyras is manufactured by Mentice Spain S.L..
What is the FDA product code for Ankyras?
The FDA product code for Ankyras is PZO.
Other Devices by Mentice Spain S.L.
Related Devices (Code: PZO)
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.