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FDA 510(k)

Triton Cage

K-Number: K183407 · 2019-08-30

ApplicantMedyssey USA, Inc.
Decision Date2019-08-30
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Triton 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 2019-08-30 under 510(k) number K183407. 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 Triton Cage?

Triton Cage is a medical device that received FDA 510(k) clearance on 2019-08-30. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K183407.

When did Triton Cage receive FDA 510(k) clearance?

Triton Cage received FDA 510(k) clearance on 2019-08-30, under 510(k) number K183407.

Who is the listed applicant for Triton 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 Triton Cage?

The FDA product code for Triton Cage is MAX.

Other records listing Medyssey USA, Inc. as applicant

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Related Devices (Code: 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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