3.8mm Cs Facet Compression Device

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K052043 ↗

FDA Product Code

MRW

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• 4.5mm Bone-Lok Facet Screw, Models Tfcd-45-3040S or N; Sfcd-45-3040S or N

  Unclassified

  FDA 510(k) K043351 Active Cleared 18 Feb 2005

• Helical Compression Anchor System, Non-Cannulated

  Class II

  FDA 510(k) K012817 Active Cleared 20 Nov 2001

• Helical Compression Anchor System, Cannulated Single Helix

  Class II

  FDA 510(k) K012818 Active Cleared 20 Nov 2001

• Disposable Posterior Lumbar Stabilization Procedure Kit, Models 9045-01 and 9045-02; Compression Tool, Model 6113-00

  Unclassified

  FDA 510(k) K062391 Active Cleared 14 Sep 2006

• Titanium Compression Anchor System Model Version 2

  Class II

  FDA 510(k) K012280 Active Cleared 17 Aug 2001

• Bone-Lok Hp Washer

  Class II

  FDA 510(k) K040250 Active Cleared 23 Mar 2004

See all devices from Triage Medical, Inc. →