Kinetic Technology Precision Adjustor Mod. Shlcp-5

• • Terminated Z-0004-05 FDA Unclassified (pre-2012) ·initiated 3 Sep 2004 ·on shared 510(k) K922695

  The device has a potential risk of failure caused by faulty wiring within the electrical component. The wires can overheat and eventually break in two.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

510(k) Number

K922695 ↗

FDA Product Code

LXM

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Precision Spinal Adjuster Model 115

  Unclassified

  FDA 510(k) K870910 Active Cleared 26 Apr 1988

• Kinetic Technology Precision Adustor Model Shlcp-4

  Unclassified

  FDA 510(k) K922694 Active Cleared 30 Sep 1992

• Kinetic Technology Pocket Precision Adjustor

  Unclassified

  FDA 510(k) K922692 Active Cleared 30 Sep 1992

• Kinetic Technoogy Precision Adjustor Model Shlcp-1

  Unclassified

  FDA 510(k) K922693 Active Cleared 30 Sep 1992