MINIFIX

Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

FERGUSON MEDICAL

The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Minifix.

Pre-market Notification Details

• Device ID: K964094
• 510k Number: K964094
• Device Name: MINIFIX
• Classification: Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
• Applicant: FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619
• Contact: Frank Ferguson
• Correspondent: Frank Ferguson; FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619
• Product Code: KTT
• CFR Regulation Number: 888.3030 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-10-11
• Decision Date: 1996-11-27
• Summary: summary