Mcconnell Orthopedic U-Hook Assembly

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

510(k) Number

K871822 ↗

FDA Product Code

FWZ

Device Class

Class I

Regulation

21 CFR Part 878.4950

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Lateral Buttress Support

  Class I

  FDA 510(k) K905565 Active Cleared 21 Feb 1991

• Mcconnell Orthopedic Universal Positioner (Mup)

  Class I

  FDA 510(k) K871803 Active Cleared 19 May 1987

• Mcconnell Orthopedic Shoulder/Hip Positioner

  Class I

  FDA 510(k) K871819 Active Cleared 22 May 1987

• Mcconnel Orthopedic Arthroscopy Support Assembly

  Class I

  FDA 510(k) K871804 Active Cleared 19 May 1987

• Mcconnell Shoulder Brace

  Class I

  FDA 510(k) K910974 Active Cleared 21 Mar 1991

• Mcconnell Orthopedic Tibial Positioner

  Class I

  FDA 510(k) K871823 Active Cleared 26 May 1987

See all devices from Mcconnell Orthopedic →