MectaLIF Anterior Lag Extension
K-Number: K232123 · 2023-10-18
ApplicantMedacta International S.A.
Decision Date2023-10-18
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MectaLIF Anterior Lag Extension is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2023-10-18 under approval number K232123. 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 Anterior Lag Extension?
MectaLIF Anterior Lag Extension is a medical device that received FDA 510(k) clearance on 2023-10-18. It is manufactured by Medacta International S.A.. The 510(k) number is K232123.
When was MectaLIF Anterior Lag Extension approved by the FDA?
MectaLIF Anterior Lag Extension received FDA 510(k) clearance on 2023-10-18, under approval number K232123.
What company makes MectaLIF Anterior Lag Extension?
MectaLIF Anterior Lag Extension is manufactured by Medacta International S.A..
What is the FDA product code for MectaLIF Anterior Lag Extension?
The FDA product code for MectaLIF Anterior Lag Extension is OVD.
Related Clinical Trials
Other Devices by Medacta International S.A.
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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.