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FDA 510(k)

SUPERTILT PLUS (STP)

K-Number: K221435 · 2022-10-28

ApplicantPower Plus Mobility
Decision Date2022-10-28
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPERTILT PLUS (STP) is a medical device manufactured by Power Plus Mobility. It received FDA 510(k) clearance on 2022-10-28 under approval number K221435. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERTILT PLUS (STP)?

SUPERTILT PLUS (STP) is a medical device that received FDA 510(k) clearance on 2022-10-28. It is manufactured by Power Plus Mobility. The 510(k) number is K221435.

When was SUPERTILT PLUS (STP) approved by the FDA?

SUPERTILT PLUS (STP) received FDA 510(k) clearance on 2022-10-28, under approval number K221435.

What company makes SUPERTILT PLUS (STP)?

SUPERTILT PLUS (STP) is manufactured by Power Plus Mobility.

What is the FDA product code for SUPERTILT PLUS (STP)?

The FDA product code for SUPERTILT PLUS (STP) is IOR.

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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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