Zavation Cervical Plate System

Appliance, Fixation, Spinal Intervertebral Body

Zavation Medical Products LLC

The following data is part of a premarket notification filed by Zavation Medical Products Llc with the FDA for Zavation Cervical Plate System.

Pre-market Notification Details

• Device ID: K181244
• 510k Number: K181244
• Device Name: Zavation Cervical Plate System
• Classification: Appliance, Fixation, Spinal Intervertebral Body
• Applicant: Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232
• Contact: Matt Jones
• Correspondent: Matt Jones; Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232
• Product Code: KWQ
• CFR Regulation Number: 888.3060 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2018-05-10
• Decision Date: 2018-07-10
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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