M. Kurosaka Interference Fixation Screw

• • Terminated Z-0696-03 FDA Unclassified (pre-2012) ·initiated 28 Feb 2003

  Mislabeled product: Screw length incorrectly labeled may contain a 20 mm instead of 30 mm.

• • Terminated Z-0697-03 FDA Unclassified (pre-2012) ·initiated 28 Feb 2003

  Mislabeled product: Screw length incorrectly labeled may contain a 20 mm instead of 30 mm

510(k) Number

K933738 ↗

FDA Product Code

HWC

Device Class

Class II

Regulation

21 CFR Part 888.3040

Advisory Committee

Orthopedic

FDA Decision

SN

• Delta Shoulder

  Class II

  FDA 510(k) K021478 Active Cleared 18 Nov 2003

• Synatomic Revision Femoral Prosthesis

  Class II

  FDA 510(k) K860594 Active Cleared 14 Mar 1986

• Porocoat (R) Proximal Femoral Third Prosthesis

  Class II

  FDA 510(k) K872025 Active Cleared 18 Aug 1987

• Cobalt Chrome Gemini

  Class II

  FDA 510(k) K934909 Active Cleared 28 Apr 1994

• Depuy Titanium Cross Pin Fixation System

  Class II

  FDA 510(k) K954630 Active Cleared 13 Dec 1995

• Depuy Cannulated Cross Pin Screw System

  Class II

  FDA 510(k) K963973 Active Cleared 16 Dec 1996

See all devices from Depuy, Inc. →