PPP
- Product code
- PPP
- Device name
- Disposable Joint Aspiration/Injection Kit
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- Enforcement Discretion
FDA classification definition
This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.Fda.Gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080217.Pdf.This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Official FDA classification page: PPP
Classification and pathway per current FDA publications. Data from openFDA (CC0).