Mg OSTEOREVIVE, Mg OSTEOCRETE
K-Number: K242372 · 2024-10-18
ApplicantBone Solutions, Inc.
Decision Date2024-10-18
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Mg OSTEOREVIVE, Mg OSTEOCRETE is a medical device manufactured by Bone Solutions, Inc.. It received FDA 510(k) clearance on 2024-10-18 under approval number K242372. 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 OSTEOREVIVE, Mg OSTEOCRETE?
Mg OSTEOREVIVE, Mg OSTEOCRETE is a medical device that received FDA 510(k) clearance on 2024-10-18. It is manufactured by Bone Solutions, Inc.. The 510(k) number is K242372.
When was Mg OSTEOREVIVE, Mg OSTEOCRETE approved by the FDA?
Mg OSTEOREVIVE, Mg OSTEOCRETE received FDA 510(k) clearance on 2024-10-18, under approval number K242372.
What company makes Mg OSTEOREVIVE, Mg OSTEOCRETE?
Mg OSTEOREVIVE, Mg OSTEOCRETE is manufactured by Bone Solutions, Inc..
What is the FDA product code for Mg OSTEOREVIVE, Mg OSTEOCRETE?
The FDA product code for Mg OSTEOREVIVE, Mg OSTEOCRETE 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.