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 a medical device manufactured by Medyssey USA, Inc.. It received FDA 510(k) clearance on 2017-12-14 under approval 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. It is manufactured by Medyssey USA, Inc.. The 510(k) number is K170389.
When was TAURUS PEEK Cage System approved by the FDA?
TAURUS PEEK Cage System received FDA 510(k) clearance on 2017-12-14, under approval number K170389.
What company makes TAURUS PEEK Cage System?
TAURUS PEEK Cage System is manufactured by Medyssey USA, Inc..
What is the FDA product code for TAURUS PEEK Cage System?
The FDA product code for TAURUS PEEK Cage System is MAX.
Other Devices by Medyssey USA, Inc.
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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.