FDA-recognized standard · Orthopedic
ASTM F1820: Standard Test Method for Determining the Forces for Disassembly of Modular Acetabular Devices
Yes. FDA recognizes ASTM F1820-22 as recognition 11-394, entered 2022-12-19.
Recognized editions of ASTM F1820
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 11-394 | ASTM F1820-22 | 2022-12-19 | Complete | — |
Regulations
FDA lists these classification regulations against ASTM F1820: 21 CFR 888.3300, 21 CFR 888.3310, 21 CFR 888.3320, 21 CFR 888.3330, 21 CFR 888.3340, 21 CFR 888.3350, 21 CFR 888.3353, 21 CFR 888.3358, 21 CFR 888.3360, 21 CFR 888.3370, 21 CFR 888.3380, 21 CFR 888.3410.
Product codes that cite ASTM F1820
24 FDA product codes cite ASTM F1820, including JDH, JDI, JDL, KMC, KWA.
- JDH
- JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- JDL
- KMC
- KWA
- KWB
- KWZ
- KXB
- KXD
- LPF
- LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- LWJ
- LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- MAY
- MBL
- MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- MRA
- NXT
- OCG
- OQG
- OQH
- OQI
- OVO
- PBI
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.