Bacfix Spinal Fixation System

• • Terminated Z-0920-04 FDA Unclassified (pre-2012) ·initiated 1 Apr 2002

  The instrument can break during surgery causing delay of surgery and/or fragments in the surgical site.

510(k) Number

K964404 ↗

FDA Product Code

KWP

Device Class

Class II

Regulation

21 CFR Part 888.3050

Advisory Committee

Orthopedic

FDA Decision

SN

• Spinal Concepts, Inc. Insight Pedicle Screw System

  Class II

  FDA 510(k) K031855 Active Cleared 17 Sep 2003

• Universal Bone Plate III System (Ubp III)

  Class II

  FDA 510(k) K020611 Active Cleared 27 Mar 2002

• Modification to Incompass Spinal Fixation System

  Class II

  FDA 510(k) K023644 Active Cleared 25 Nov 2002

• Spinal Concepts, Inc., Universal Bone Plate System II

  Class II

  FDA 510(k) K973586 Active Cleared 7 Nov 1997

• Spinal Concepts Cadence and Traxis

  Class II

  FDA 510(k) K033517 Active Cleared 18 Feb 2004

• Harmony Port System, Model 1907 Series

  Class II

  FDA 510(k) K050706 Active Cleared 15 Apr 2005

See all devices from Spinal Concepts, Inc. →