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FDA 510(k)

Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm

K-Number: K173709 · 2018-01-26

ApplicantInneuroco, Inc.
Decision Date2018-01-26
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm is the device name listed in this FDA 510(k) record. The listed applicant is Inneuroco, Inc.. It received FDA 510(k) clearance on 2018-01-26 under 510(k) number K173709. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm?

Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm is a medical device that received FDA 510(k) clearance on 2018-01-26. The listed applicant is Inneuroco, Inc.. The 510(k) number is K173709.

When did Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm receive FDA 510(k) clearance?

Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm received FDA 510(k) clearance on 2018-01-26, under 510(k) number K173709.

Who is the listed applicant for Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm?

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

What is the FDA product code for Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm?

The FDA product code for Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm is DQY.

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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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