Vericore Gradient Temporary Disc
K-Number: K152443 · 2016-05-11
ApplicantWhip Mix Corporation
Decision Date2016-05-11
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Vericore Gradient Temporary Disc is a medical device manufactured by Whip Mix Corporation. It received FDA 510(k) clearance on 2016-05-11 under approval number K152443. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vericore Gradient Temporary Disc?
Vericore Gradient Temporary Disc is a medical device that received FDA 510(k) clearance on 2016-05-11. It is manufactured by Whip Mix Corporation. The 510(k) number is K152443.
When was Vericore Gradient Temporary Disc approved by the FDA?
Vericore Gradient Temporary Disc received FDA 510(k) clearance on 2016-05-11, under approval number K152443.
What company makes Vericore Gradient Temporary Disc?
Vericore Gradient Temporary Disc is manufactured by Whip Mix Corporation.
What is the FDA product code for Vericore Gradient Temporary Disc?
The FDA product code for Vericore Gradient Temporary Disc is EBG.
Other Devices by Whip Mix Corporation
Related Devices (Code: EBG)
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.