Mcconnell Shoulder Brace

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K910974 ↗

FDA Product Code

IQI

Device Class

Class I

Regulation

21 CFR Part 890.3475

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Mcconnell Orthopedic U-Hook Assembly

  Class I

  FDA 510(k) K871822 Active Cleared 26 May 1987

• 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 Orthopedic Tibial Positioner

  Class I

  FDA 510(k) K871823 Active Cleared 26 May 1987

See all devices from Mcconnell Orthopedic →