FDA-recognized standard · Orthopedic
ASTM F2777: Standard Test Method for Evaluating Knee Bearing (Tibial Insert) Endurance and Deformation Under High Flexion
Yes. FDA recognizes ASTM F2777-23 as recognition 11-408, entered 2023-12-18.
Recognized editions of ASTM F2777
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 11-408 | ASTM F2777-23 | 2023-12-18 | Complete | — |
Regulations
FDA lists these classification regulations against ASTM F2777: 21 CFR 888.3490, 21 CFR 888.3500, 21 CFR 888.3520, 21 CFR 888.3530, 21 CFR 888.3535, 21 CFR 888.3560, 21 CFR 888.3565.
Product codes that cite ASTM F2777
16 FDA product codes cite ASTM F2777, including HRY, HSX, JWH, KMB, KTX.
- HRY
- HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
- JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- KMB
- KTX
- KYK
- LGE
- LXY
- MBD
- MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- MBV
- NJD
- NJL
- NPJ
- NRA
- OIY
Source: FDA Recognized Consensus Standards database, snapshot of 2026-09-01. Search every recognition in the Consensus Standards Lookup, or browse all standards with a page.