DeviceSignal · 510(k) cleared
Bone Solutions, Inc.
FDA 510(k) decision recorded 2026-09-11 · K262230 · Traditional 510(k)
Event510(k) cleared
Effective2026-09-11
DecisionSESE
On 2026-09-11 the FDA recorded a 510(k) clearance decision for Bone Solutions, Inc., for Mg OSTEOREVIVE;Mg OSTEOCRETE. Clearance K262230. Product code MQV. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K262230
- Applicant
- Bone Solutions, Inc.
- Device
- Mg OSTEOREVIVE;Mg OSTEOCRETE
- Decided on
- 2026-09-11
- Received on
- 2026-06-30
- Decision
- SESE
- Clearance type
- Traditional
- Product code
- MQV
- Review days
- 73
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K262230- Snapshot hash
a3a25028eeae44912b95531a87efac5a606d6a01c346404e56e7ec7fd97b2d35- Source URL
- https://download.open.fda.gov/device/510k/device-510k-0001-of-0001.json.zip
- Observed
- 2026-09-23T12:43:31.676Z
- Transform
fda_device_510k_to_clearance v1- Event rule
fda_device_510k_cleared v1- Event key
400328e9920128ca43db4270bcac4bbf64a2ad1c021da55daa43e830b6732cda- Signal type
device_clearance.granted
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)