Orthobond Mariner Pedicle Screw System— 510(k) DEN220015
UnknownOrthobond Coporation
FDA 510(k) clearance DEN220015 for Orthobond Mariner Pedicle Screw System, Unknown on 2024-04-05. Applicant: Orthobond Coporation. Device class: 2.
Clearance details
- Applicant
- Orthobond Coporation
- Product code
- Code QZY
- Device class
- Class 2
- Regulation
- 21 CFR 888.3071
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Monmouth, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.