MectaLIF Posterior Extension
K-Number: K181970 · 2018-12-04
ApplicantMedacta International S.A.
Decision Date2018-12-04
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MectaLIF Posterior Extension is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2018-12-04 under approval number K181970. 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 Posterior Extension?
MectaLIF Posterior Extension is a medical device that received FDA 510(k) clearance on 2018-12-04. It is manufactured by Medacta International S.A.. The 510(k) number is K181970.
When was MectaLIF Posterior Extension approved by the FDA?
MectaLIF Posterior Extension received FDA 510(k) clearance on 2018-12-04, under approval number K181970.
What company makes MectaLIF Posterior Extension?
MectaLIF Posterior Extension is manufactured by Medacta International S.A..
What is the FDA product code for MectaLIF Posterior Extension?
The FDA product code for MectaLIF Posterior 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.