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FDA 510(k)

TAURUS PEEK Cage System

K-Number: K170389 · 2017-12-14

ApplicantMedyssey USA, Inc.
Decision Date2017-12-14
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TAURUS PEEK Cage System 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 2017-12-14 under 510(k) number K170389. 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 TAURUS PEEK Cage System?

TAURUS PEEK Cage System is a medical device that received FDA 510(k) clearance on 2017-12-14. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K170389.

When did TAURUS PEEK Cage System receive FDA 510(k) clearance?

TAURUS PEEK Cage System received FDA 510(k) clearance on 2017-12-14, under 510(k) number K170389.

Who is the listed applicant for TAURUS PEEK Cage System?

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 TAURUS PEEK Cage System?

The FDA product code for TAURUS PEEK Cage System 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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