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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 the device name listed in this FDA 510(k) record. The listed applicant is Power Plus Mobility. It received FDA 510(k) clearance on 2022-10-28 under 510(k) 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. The listed applicant is Power Plus Mobility. The 510(k) number is K221435.

When did SUPERTILT PLUS (STP) receive FDA 510(k) clearance?

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

Who is the listed applicant for SUPERTILT PLUS (STP)?

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

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

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

Related Devices (Code: IOR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261571Manual Wheelchair (H008, PCK7)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.K252370GEN 4 JOY WheelchairFree Wheelchair MissionK261076Caregiver-assisted wheelchair (MS02);Caregiver-assisted wheelchair (MA02)GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.K261075Manual Wheelchair (MS01);Manual Wheelchair (MA01)GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.K260849ICON 35; ICON 45; ICON 60; ICON 30FAFRehasense USA, Inc.K260642Manual Wheelchair (LW01108)Anhui Longway Medical Technology Co., Ltd.

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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