Osteoboost Belt— 510(k) DEN230015
UnknownBone Health Technologies, Inc.
FDA 510(k) clearance DEN230015 for Osteoboost Belt, Unknown on 2024-01-12. Applicant: Bone Health Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Bone Health Technologies, Inc.
- Product code
- Code QZO
- Device class
- Class 2
- Regulation
- 21 CFR 888.5895
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Redwood City, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.