MectaLIF Extension
K-Number: K212831 · 2021-10-29
ApplicantMedacta International S.A.
Decision Date2021-10-29
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MectaLIF Extension is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2021-10-29 under approval number K212831. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MectaLIF Extension?
MectaLIF Extension is a medical device that received FDA 510(k) clearance on 2021-10-29. It is manufactured by Medacta International S.A.. The 510(k) number is K212831.
When was MectaLIF Extension approved by the FDA?
MectaLIF Extension received FDA 510(k) clearance on 2021-10-29, under approval number K212831.
What company makes MectaLIF Extension?
MectaLIF Extension is manufactured by Medacta International S.A..
What is the FDA product code for MectaLIF Extension?
The FDA product code for MectaLIF Extension is MAX.
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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.