Parcus SLiK Fix Screw
K-Number: K170877 · 2017-06-02
ApplicantParcus Medical
Decision Date2017-06-02
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Parcus SLiK Fix Screw is a medical device manufactured by Parcus Medical. It received FDA 510(k) clearance on 2017-06-02 under approval number K170877. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Parcus SLiK Fix Screw?
Parcus SLiK Fix Screw is a medical device that received FDA 510(k) clearance on 2017-06-02. It is manufactured by Parcus Medical. The 510(k) number is K170877.
When was Parcus SLiK Fix Screw approved by the FDA?
Parcus SLiK Fix Screw received FDA 510(k) clearance on 2017-06-02, under approval number K170877.
What company makes Parcus SLiK Fix Screw?
Parcus SLiK Fix Screw is manufactured by Parcus Medical.
What is the FDA product code for Parcus SLiK Fix Screw?
The FDA product code for Parcus SLiK Fix Screw is MBI.
Other Devices by Parcus Medical
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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.