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FDA 510(k)

Varian cage

K-Number: K172756 · 2017-12-08

ApplicantMedyssey USA, Inc.
Decision Date2017-12-08
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Varian cage is the device name listed in this FDA 510(k) record. The listed applicant is Medyssey USA, Inc.. It received FDA 510(k) clearance on 2017-12-08 under 510(k) number K172756. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Varian cage?

Varian cage is a medical device that received FDA 510(k) clearance on 2017-12-08. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K172756.

When did Varian cage receive FDA 510(k) clearance?

Varian cage received FDA 510(k) clearance on 2017-12-08, under 510(k) number K172756.

Who is the listed applicant for Varian cage?

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

What is the FDA product code for Varian cage?

The FDA product code for Varian cage is MAX.

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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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