KIJ
- Product code
- KIJ
- Device name
- Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4820
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 29
Official FDA classification page: KIJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).