Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Biomet, Inc.. It received FDA 510(k) clearance on 2017-03-31 under approval 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. It is manufactured by Biomet, Inc.. The 510(k) number is K162559.

When was Move Forward 3D Motion Simulation Service approved by the FDA?

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

What company makes Move Forward 3D Motion Simulation Service?

Move Forward 3D Motion Simulation Service is manufactured by Biomet, Inc..

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.

Related Clinical Trials

NCT07382674 Zesty Exercise System for Therapeutic Engagement RECRUITING NCT07593781 rESWT vs LLLT for Cervical Myofascial Pain COMPLETED NCT06236516 One Fraction Simulation-Free Treatment With CT-Guided Stereotactic Adaptive Radiotherapy for Patients With Oligometastatic and Primary Lung Tumors COMPLETED NCT07539272 Device for Driving Simulation for the Rehabilitation of Balance and Proprioception NOT_YET_RECRUITING NCT07527845 Feasibility of an Augmented Reality Novel Approach for the Rehabilitation of Chronic Low Back Pain Patients With Kinesiophobia COMPLETED

Other Devices by Biomet, Inc.

K161592Persona Partial Knee System K162424Ulna Plating System K161166StageOne Select Cement Spacer Molds for Temporary Hip Replacement K160071StageOne Disposable Cement Spacer Molds for Temporary Hemi-Shoulder Prosthesis K161190G7 Dual Mobility System, Active Articulation System K153657Vanguard XP Knee System

View all 34 devices →

Related Devices (Code: LLZ)

K161959ClearView cCADClearview Diagnostics, Inc. K163539Ez3D-i / E3Ewoosoft Co., Ltd. K162955Multi-Modality Tumor Tracking (MMTT) applicationPhilips Medical Systems Nederland B.V. K160852ZiaZetta Medical Technologies, LLC K162376CAAS MR 4D FlowPie Medical Imaging BV K161322CT CoPilotZepmed, LLC

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.

↑