PPR — Surgical Cannulaes & Depth Gauge Kit For Arthroscopic Procedures Class II

FDA Device Classification

FDA product code PPR covers "Surgical Cannulaes & Depth Gauge Kit For Arthroscopic Procedures", a Class II medical device regulated under 21 CFR 888.1100. Submissions are reviewed by the Orthopedic panel.

Classification Details

Product Code
PPR
Device Class
Class II
Regulation Number
888.1100
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

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.