Product code MNU— Orthopedic
OSSIOfiber® Compression Staple
- Classification name
- Staple, Absorbable
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code MNU
FDA has cleared devices under product code MNU between 2001 and 2024, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2024
- 2023
- 2022
- 2001
Top applicants under product code MNU
Recent clearances under product code MNU
Data sourced from openFDA. This site is unofficial and independent of the FDA.