Neonail 932.013
by Neoortho Produtos Ortopédicos S/A.
Neonail 932.013 is a Class II device made by Neoortho Produtos Ortopédicos S/A., cleared under FDA 510(k) K141103 on 23 Sep 2014 and listed in FDA GUDID since 30 Sep 2015 (UDI-DI 07899893202997), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07899893202997 | Date30 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141103 | Date23 Sep 2014 | StatusActive |
Official records
- AccessGUDID record 07899893202997
- FDA 510(k) database K141103
Across registries
- FDA 510(k) K141103 decided 23 Sep 2014 Active
- FDA GUDID UDI-DI 07899893202997 listed 30 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K141103
- Listed FDA GUDID 07899893202997
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Neonail
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Model / reference
- 932.013
- Primary DI / UDI-DI
- 07899893202997
- 510(k) Number
- FDA product code
- HSB
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Device class
- Class II
- Regulation number
- 888.3020
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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