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FDA 510(k)

Move Forward 3D Motion Simulation Service

K-Number: K162559 · 2017-03-31

ApplicantBiomet, Inc.
Decision Date2017-03-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Move Forward 3D Motion Simulation Service is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2017-03-31 under 510(k) number K162559. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Move Forward 3D Motion Simulation Service?

Move Forward 3D Motion Simulation Service is a medical device that received FDA 510(k) clearance on 2017-03-31. The listed applicant is Biomet, Inc.. The 510(k) number is K162559.

When did Move Forward 3D Motion Simulation Service receive FDA 510(k) clearance?

Move Forward 3D Motion Simulation Service received FDA 510(k) clearance on 2017-03-31, under 510(k) number K162559.

Who is the listed applicant for Move Forward 3D Motion Simulation Service?

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

What is the FDA product code for Move Forward 3D Motion Simulation Service?

The FDA product code for Move Forward 3D Motion Simulation Service is LLZ.

Other records listing Biomet, Inc. as applicant

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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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