Mg OSTEOINJECT
K-Number: K221256 · 2022-06-28
ApplicantBone Solutions, Inc.
Decision Date2022-06-28
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Mg OSTEOINJECT is a medical device manufactured by Bone Solutions, Inc.. It received FDA 510(k) clearance on 2022-06-28 under approval number K221256. 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 Mg OSTEOINJECT?
Mg OSTEOINJECT is a medical device that received FDA 510(k) clearance on 2022-06-28. It is manufactured by Bone Solutions, Inc.. The 510(k) number is K221256.
When was Mg OSTEOINJECT approved by the FDA?
Mg OSTEOINJECT received FDA 510(k) clearance on 2022-06-28, under approval number K221256.
What company makes Mg OSTEOINJECT?
Mg OSTEOINJECT is manufactured by Bone Solutions, Inc..
What is the FDA product code for Mg OSTEOINJECT?
The FDA product code for Mg OSTEOINJECT is MQV.
Other Devices by Bone Solutions, Inc.
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.