Cerament Bone Void Filler
K-Number: K240459 · 2024-03-05
ApplicantBonesupport AB
Decision Date2024-03-05
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Cerament Bone Void Filler is a medical device manufactured by Bonesupport AB. It received FDA 510(k) clearance on 2024-03-05 under approval number K240459. 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 Cerament Bone Void Filler?
Cerament Bone Void Filler is a medical device that received FDA 510(k) clearance on 2024-03-05. It is manufactured by Bonesupport AB. The 510(k) number is K240459.
When was Cerament Bone Void Filler approved by the FDA?
Cerament Bone Void Filler received FDA 510(k) clearance on 2024-03-05, under approval number K240459.
What company makes Cerament Bone Void Filler?
Cerament Bone Void Filler is manufactured by Bonesupport AB.
What is the FDA product code for Cerament Bone Void Filler?
The FDA product code for Cerament Bone Void Filler is MQV.
Other Devices by Bonesupport AB
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.