FDA-recognized standard · Orthopedic
ASTM F3292: Standard Practice for Inspection of Spinal Implants Undergoing Testing
Yes. FDA recognizes ASTM F3292-25 as recognition 11-435, entered 2025-12-22. FDA also lists ASTM F3292-19 (recognition 11-369, transition period ending 2027-12-19).
Recognized editions of ASTM F3292
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 11-435 | ASTM F3292-25 | 2025-12-22 | Complete | — |
| 11-369 | ASTM F3292-19 | 2020-07-06 | Complete | 2027-12-19 |
Regulations
FDA lists these classification regulations against ASTM F3292: 21 CFR 888.3050, 21 CFR 888.3060, 21 CFR 888.3070, 21 CFR 888.3075, 21 CFR 888.3080.
Product codes that cite ASTM F3292
12 FDA product codes cite ASTM F3292, including KWP, KWQ, MAX, MJO, MNH.
- KWP
- KWQ Appliance, Fixation, Spinal Intervertebral Body
- MAX Intervertebral Fusion Device With Bone Graft, Lumbar
- MJO
- MNH
- MNI
- MQP Spinal Vertebral Body Replacement Device
- NKB Thoracolumbosacral Pedicle Screw System
- NKG Posterior Cervical Screw System
- ODP Intervertebral Fusion Device With Bone Graft, Cervical
- OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
- OVE Intervertebral Fusion Device With Integrated Fixation, 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.