FDA-recognized standard · Orthopedic
ASTM F2267: Standard Test Method for Measuring Load-Induced Subsidence of Intervertebral Body Fusion Device Under Static Axial Compression
Yes. FDA recognizes ASTM F2267-24 as recognition 11-423, entered 2025-12-22. FDA also lists ASTM F2267-04 (Reapproved 2018) (recognition 11-185, transition period ending 2027-12-19).
Recognized editions of ASTM F2267
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 11-423 | ASTM F2267-24 | 2025-12-22 | Complete | — |
| 11-185 | ASTM F2267-04 (Reapproved 2018) | 2018-09-17 | Complete | 2027-12-19 |
Regulations
FDA lists these classification regulations against ASTM F2267: 21 CFR 888.3060, 21 CFR 888.3080.
Product codes that cite ASTM F2267
8 FDA product codes cite ASTM F2267, including MAX, MJO, MQP, ODP, OVD.
- MAX Intervertebral Fusion Device With Bone Graft, Lumbar
- MJO
- MQP Spinal Vertebral Body Replacement Device
- ODP Intervertebral Fusion Device With Bone Graft, Cervical
- OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
- OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
- PHM
- PLR Spinal Vertebral Body Replacement Device - Cervical
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.