Rounded Cannulated Inside-Out (Rci) Acl Screw

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

510(k) Number

K945687 ↗

FDA Product Code

HWC

Device Class

Class II

Regulation

21 CFR Part 888.3040

Advisory Committee

Orthopedic

FDA Decision

SN

• Aims Cannulated ACL Screw (7MM Diameter)

  Class II

  FDA 510(k) K945236 Active Cleared 3 Feb 1995

• Musclemax Plus Electrical Muscle Stimulator

  Class II

  FDA 510(k) K962462 Active Cleared 23 Sep 1996

• Brace Neutralizer

  Class II

  FDA 510(k) K932592 Active Cleared 18 Mar 1994

• Protective Restraint

  Class I

  FDA 510(k) K963492 Active Cleared 12 Nov 1996

• Musclesense Electromyography Device

  Class II

  FDA 510(k) K951350 Active Cleared 23 Jun 1995

• Rounded Cannulated Inside-Out (Rci) Acl Screw

  Class II

  FDA 510(k) K932862 Active Cleared 10 Mar 1994

See all devices from Smith and Nephew Donjoy, Inc. →