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FDA 510(k)

MectaLIF 3D Metal Anterior

K-Number: K254202 · 2026-05-05

ApplicantMedacta International S.A.
Decision Date2026-05-05
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MectaLIF 3D Metal Anterior is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2026-05-05 under approval number K254202. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MectaLIF 3D Metal Anterior?

MectaLIF 3D Metal Anterior is a medical device that received FDA 510(k) clearance on 2026-05-05. It is manufactured by Medacta International S.A.. The 510(k) number is K254202.

When was MectaLIF 3D Metal Anterior approved by the FDA?

MectaLIF 3D Metal Anterior received FDA 510(k) clearance on 2026-05-05, under approval number K254202.

What company makes MectaLIF 3D Metal Anterior?

MectaLIF 3D Metal Anterior is manufactured by Medacta International S.A..

What is the FDA product code for MectaLIF 3D Metal Anterior?

The FDA product code for MectaLIF 3D Metal Anterior is OVD.

Other Devices by Medacta International S.A.

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Related Devices (Code: OVD)

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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.

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