OsteoCNX
K-Number: K223563 · 2023-01-25
ApplicantConverg Engineering
Decision Date2023-01-25
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
OsteoCNX is a medical device manufactured by Converg Engineering. It received FDA 510(k) clearance on 2023-01-25 under approval number K223563. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the OsteoCNX?
OsteoCNX is a medical device that received FDA 510(k) clearance on 2023-01-25. It is manufactured by Converg Engineering. The 510(k) number is K223563.
When was OsteoCNX approved by the FDA?
OsteoCNX received FDA 510(k) clearance on 2023-01-25, under approval number K223563.
What company makes OsteoCNX?
OsteoCNX is manufactured by Converg Engineering.
What is the FDA product code for OsteoCNX?
The FDA product code for OsteoCNX is MQV.
Related Devices (Code: MQV)
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.