266-8520
266-8520 is a Class II device made by Ortho Development Corp., listed in FDA GUDID since 1 Nov 2023 (UDI-DI 00822409122325), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00822409122325 | Date1 Nov 2023 | StatusListed |
Official records
- AccessGUDID record 00822409122325
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Knee tibia prosthesis trial, reusable
- Model / reference
- 266-8520
- Description
- PS Plus Insert Trial Size 5 20mm
- Primary DI / UDI-DI
- 00822409122325
- FDA product code
- JWH
- GMDN term
- Knee tibia prosthesis trial, reusable
- Device class
- Class II
- Regulation number
- 888.3560
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Height — 20 Millimeter
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