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FDA 510(k)

MPACT DM LINER CONVERTER

K-Number: K131458 · 2013-10-01

ApplicantMedacta International
Decision Date2013-10-01
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MPACT DM LINER CONVERTER is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International. It received FDA 510(k) clearance on 2013-10-01 under 510(k) number K131458. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPACT DM LINER CONVERTER?

MPACT DM LINER CONVERTER is a medical device that received FDA 510(k) clearance on 2013-10-01. The listed applicant is Medacta International. The 510(k) number is K131458.

When did MPACT DM LINER CONVERTER receive FDA 510(k) clearance?

MPACT DM LINER CONVERTER received FDA 510(k) clearance on 2013-10-01, under 510(k) number K131458.

Who is the listed applicant for MPACT DM LINER CONVERTER?

The FDA 510(k) record lists Medacta International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPACT DM LINER CONVERTER?

The FDA product code for MPACT DM LINER CONVERTER is LZO.

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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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