AccuFill Bone Substitute Material
K-Number: K190814 · 2019-06-10
ApplicantZimmer Knee Creations
Decision Date2019-06-10
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
AccuFill Bone Substitute Material is a medical device manufactured by Zimmer Knee Creations. It received FDA 510(k) clearance on 2019-06-10 under approval number K190814. 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 AccuFill Bone Substitute Material?
AccuFill Bone Substitute Material is a medical device that received FDA 510(k) clearance on 2019-06-10. It is manufactured by Zimmer Knee Creations. The 510(k) number is K190814.
When was AccuFill Bone Substitute Material approved by the FDA?
AccuFill Bone Substitute Material received FDA 510(k) clearance on 2019-06-10, under approval number K190814.
What company makes AccuFill Bone Substitute Material?
AccuFill Bone Substitute Material is manufactured by Zimmer Knee Creations.
What is the FDA product code for AccuFill Bone Substitute Material?
The FDA product code for AccuFill Bone Substitute Material is MQV.
Related Clinical Trials
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.