Jackson Multipurpose Operating Table

• • Terminated Z-0073-2012 FDA Unclassified (pre-2012) ·initiated 29 Jul 2011

  Reports of injury related incidents while using the Mizuho OSI Modular Table System.

510(k) Number

K910736 ↗

FDA Product Code

JEA

Device Class

Class I

Regulation

21 CFR Part 878.4960

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Blakemore Retainer

  Class II

  FDA 510(k) K880253 Active Cleared 11 Mar 1988

• Extremity Elevator

  Class I

  FDA 510(k) K870125 Active Cleared 4 Feb 1987

• Tendon Leader

  Not classified

  FDA 510(k) K853764 Active Cleared 7 Oct 1985

• Freeman Total Hip System Ridged Stem

  Class II

  FDA 510(k) K890331 Active Cleared 13 Oct 1989

• Osi Rizzoli Trauma Table (Electric Version)

  Class I

  FDA 510(k) K881060 Active Cleared 25 Mar 1988

• Tlc Support Products

  Not classified

  FDA 510(k) K803029 Active Cleared 22 Dec 1980

See all devices from Orthopedic Systems, Inc. →