FDA-recognized standard · Materials
ASTM F3333: Standard Specification for Chopped Carbon Fiber Reinforced (CFR) Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications
Yes. FDA recognizes ASTM F3333-20 as recognition 8-558, entered 2021-06-07.
Recognized editions of ASTM F3333
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 8-558 | ASTM F3333-20 | 2021-06-07 | Complete | — |
Regulations
FDA lists these classification regulations against ASTM F3333: 21 CFR 882.5880, 21 CFR 888.3030, 21 CFR 888.3040, 21 CFR 888.3060, 21 CFR 888.3070, 21 CFR 888.3080.
Product codes that cite ASTM F3333
13 FDA product codes cite ASTM F3333, including GZB, HTY, HWC, JDW, KTT.
- GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
- HTY Pin, Fixation, Smooth
- HWC Screw, Fixation, Bone
- JDW Pin, Fixation, Threaded
- KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KWQ Appliance, Fixation, Spinal Intervertebral Body
- LWS
- MAX Intervertebral Fusion Device With Bone Graft, Lumbar
- MBI Fastener, Fixation, Nondegradable, Soft Tissue
- MQP Spinal Vertebral Body Replacement Device
- NIK
- NKB Thoracolumbosacral Pedicle Screw System
- ODP Intervertebral Fusion Device With Bone Graft, 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.