Archworx
K-Number: K173738 · 2021-02-26
ApplicantUtah Medical Products and Services
Decision Date2021-02-26
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Archworx is a medical device manufactured by Utah Medical Products and Services. It received FDA 510(k) clearance on 2021-02-26 under approval number K173738. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Archworx?
Archworx is a medical device that received FDA 510(k) clearance on 2021-02-26. It is manufactured by Utah Medical Products and Services. The 510(k) number is K173738.
When was Archworx approved by the FDA?
Archworx received FDA 510(k) clearance on 2021-02-26, under approval number K173738.
What company makes Archworx?
Archworx is manufactured by Utah Medical Products and Services.
What is the FDA product code for Archworx?
The FDA product code for Archworx is NXC.
Related Devices (Code: NXC)
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.