Palisade™ Pedicular Fixation System

Thoracolumbosacral Pedicle Screw System

Spineology Inc.

The following data is part of a premarket notification filed by Spineology Inc. with the FDA for Palisade™ Pedicular Fixation System.

Pre-market Notification Details

• Device ID: K171438
• 510k Number: K171438
• Device Name: Palisade™ Pedicular Fixation System
• Classification: Thoracolumbosacral Pedicle Screw System
• Applicant: Spineology Inc. 7800 3rd Street N., Suite 600 St. Paul, MN 55128
• Contact: Jacqueline A. Hauge
• Correspondent: Jacqueline A. Hauge; Spineology Inc. 7800 3rd Street North, Suite 600 Saint Paul, MN 55128
• Product Code: NKB
• CFR Regulation Number: 888.3070 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2017-05-16
• Decision Date: 2017-06-02
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
M7406700200	K171438	000
M7406700180	K171438	000
M7406700160	K171438	000
M7406700140	K171438	000
M7406700120	K171438	000
M7406700100	K171438	000