Medussa-PL Cage
K-Number: K200283 · 2020-06-18
ApplicantMedyssey USA, Inc.
Decision Date2020-06-18
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Medussa-PL Cage is a medical device manufactured by Medyssey USA, Inc.. It received FDA 510(k) clearance on 2020-06-18 under approval number K200283. 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 Medussa-PL Cage?
Medussa-PL Cage is a medical device that received FDA 510(k) clearance on 2020-06-18. It is manufactured by Medyssey USA, Inc.. The 510(k) number is K200283.
When was Medussa-PL Cage approved by the FDA?
Medussa-PL Cage received FDA 510(k) clearance on 2020-06-18, under approval number K200283.
What company makes Medussa-PL Cage?
Medussa-PL Cage is manufactured by Medyssey USA, Inc..
What is the FDA product code for Medussa-PL Cage?
The FDA product code for Medussa-PL 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.