Graftys Quickset
K-Number: K231714 · 2023-07-12
ApplicantGraftys
Decision Date2023-07-12
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Graftys Quickset is a medical device manufactured by Graftys. It received FDA 510(k) clearance on 2023-07-12 under approval number K231714. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Graftys Quickset?
Graftys Quickset is a medical device that received FDA 510(k) clearance on 2023-07-12. It is manufactured by Graftys. The 510(k) number is K231714.
When was Graftys Quickset approved by the FDA?
Graftys Quickset received FDA 510(k) clearance on 2023-07-12, under approval number K231714.
What company makes Graftys Quickset?
Graftys Quickset is manufactured by Graftys.
What is the FDA product code for Graftys Quickset?
The FDA product code for Graftys Quickset is MQV.
Related Devices (Code: MQV)
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.