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# Bone Solutions 510(k) Cleared for Mg Osteorevive
- URL: https://www.fdaweb.com/bone-solutions-510-k-cleared-for-mg-osteorevive/
- Published: 2022-02-02T12:00:00.000Z
- Updated: 2026-09-14T17:30:56.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5151067

FDA has cleared a Bone Solutions 510(k) for its Mg Osteorevive, a magnesium-based injectable and moldable bone void filler indicated for posterolateral spine fusion procedures. The company says that magnesium is a critical component for bone health and development, and plays a key role in the absorption and regulation of calcium. “Because of these characteristics, Mg Osteorevive is able to safely assimilate back into the body during the healing process as it is replaced with bone,” it says.