FDA 510(k)

Frontier Series Power Wheelchairs

K-Number: K213090 · 2021-11-19

Decision Date2021-11-19

Product CodeITI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Frontier Series Power Wheelchairs is a medical device manufactured by Magic Mobility. It received FDA 510(k) clearance on 2021-11-19 under approval number K213090. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Frontier Series Power Wheelchairs?

Frontier Series Power Wheelchairs is a medical device that received FDA 510(k) clearance on 2021-11-19. It is manufactured by Magic Mobility. The 510(k) number is K213090.

When was Frontier Series Power Wheelchairs approved by the FDA?

Frontier Series Power Wheelchairs received FDA 510(k) clearance on 2021-11-19, under approval number K213090.

What company makes Frontier Series Power Wheelchairs?

Frontier Series Power Wheelchairs is manufactured by Magic Mobility.

What is the FDA product code for Frontier Series Power Wheelchairs?

The FDA product code for Frontier Series Power Wheelchairs is ITI.

Other Devices by Magic Mobility

K211574Extreme X8 K203083Magic 360 Power Wheelchair K233877XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.