KTD
- Product code
- KTD
- Device name
- Orthosis, Abdominal
- Device class
- Class 1
- 21 CFR
- 21 CFR 890.3490
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
- 510(k) clearances (last 3 years)
- 3
Official FDA classification page: KTD
Classification and pathway per current FDA publications. Data from openFDA (CC0).