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FDA 510(k)

WRIGHT GRADIENT 52 - TORSO

K-Number: K131387 · 2013-11-20

ApplicantWright Therapy Products, Inc.
Decision Date2013-11-20
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIGHT GRADIENT 52 - TORSO is the device name listed in this FDA 510(k) record. The listed applicant is Wright Therapy Products, Inc.. It received FDA 510(k) clearance on 2013-11-20 under 510(k) number K131387. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT GRADIENT 52 - TORSO?

WRIGHT GRADIENT 52 - TORSO is a medical device that received FDA 510(k) clearance on 2013-11-20. The listed applicant is Wright Therapy Products, Inc.. The 510(k) number is K131387.

When did WRIGHT GRADIENT 52 - TORSO receive FDA 510(k) clearance?

WRIGHT GRADIENT 52 - TORSO received FDA 510(k) clearance on 2013-11-20, under 510(k) number K131387.

Who is the listed applicant for WRIGHT GRADIENT 52 - TORSO?

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

What is the FDA product code for WRIGHT GRADIENT 52 - TORSO?

The FDA product code for WRIGHT GRADIENT 52 - TORSO is JOW.

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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.

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