OII — Arthrogram Tray Class II

FDA Device Classification

FDA product code OII covers "Arthrogram Tray", a Class II medical device regulated under 21 CFR 892.1650. Submissions are reviewed by the Radiology panel.

Classification Details

Product Code
OII
Device Class
Class II
Regulation Number
892.1650
Submission Type
Review Panel
RA
Medical Specialty
Radiology
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.