FDA 510(k)

Triton Cage

K-Number: K183407 · 2019-08-30

Decision Date2019-08-30

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Triton Cage is a medical device manufactured by Medyssey USA, Inc.. It received FDA 510(k) clearance on 2019-08-30 under approval 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. It is manufactured by Medyssey USA, Inc.. The 510(k) number is K183407.

When was Triton Cage approved by the FDA?

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

What company makes Triton Cage?

Triton Cage is manufactured by Medyssey USA, Inc..

What is the FDA product code for Triton Cage?

The FDA product code for Triton 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.