Rpx Titanium Cemnt Restrictor

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

510(k) Number

K020344 ↗

FDA Product Code

JDK

Device Class

Class II

Regulation

21 CFR Part 878.3300

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Silhouette Spinal Fixation System Modification

  Class II

  FDA 510(k) K992276 Active Cleared 1 Oct 1999

• Silhouette Spinal Fixation System

  Class II

  FDA 510(k) K993067 Active Cleared 16 Nov 1999

• Cadence Spinal Fixation System

  Class II

  FDA 510(k) K022374 Active Cleared 24 Sep 2002

• Modification to Silhouette Spinal Fixation System

  Class II

  FDA 510(k) K020196 Active Cleared 15 Feb 2002

• Modification to: Trinica Anterior Cervical Plate System

  Class II

  FDA 510(k) K012305 Active Cleared 22 Aug 2001

• Device Modification of Silhouette Spindal Fixation System

  Class II

  FDA 510(k) K012173 Active Cleared 28 Sep 2001

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