FDA 510(k)

Correx Software

K-Number: K212552 · 2021-10-12

Decision Date2021-10-12

Product CodeKTT

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Correx Software is a medical device manufactured by Vilex, LLC. It received FDA 510(k) clearance on 2021-10-12 under approval number K212552. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Correx Software?

Correx Software is a medical device that received FDA 510(k) clearance on 2021-10-12. It is manufactured by Vilex, LLC. The 510(k) number is K212552.

When was Correx Software approved by the FDA?

Correx Software received FDA 510(k) clearance on 2021-10-12, under approval number K212552.

What company makes Correx Software?

Correx Software is manufactured by Vilex, LLC.

What is the FDA product code for Correx Software?

The FDA product code for Correx Software is KTT.

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Related Devices (Code: KTT)

K160972Gexfix External FixationGexfix International Corp. K161753Hoffman LRF SystemStryker GmbH K161417DePuy Synthes MAXFRAME Multi-Axial Correction SystemSynthes USA, LLC K160830Integra External Fixation SystemAscension Orthopedics K153377Hoffmann LRF (Limb Reconstruction Frame) SystemStryker GmbH K151881X-Fix Line AdditionsVilex IN Tennessee, Inc.

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.