Porous Genesis Patellar and Stemless Tibial Comp.

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K890132 ↗

FDA Product Code

JWH

Device Class

Class II

Regulation

21 CFR Part 888.3560

Advisory Committee

Orthopedic

FDA Decision

SN

• Richards Intra-Articular Shaver Motor

  Class I

  FDA 510(k) K842475 Active Cleared 17 Sep 1984

• Hip Continuous Passive Motion Machine

  Class I

  FDA 510(k) K862314 Active Cleared 15 Jul 1986

• U-Impulse Air Conduction in-the-Canal Hearing Aid

  Class I

  FDA 510(k) K873560 Active Cleared 29 Sep 1987

• Omni Itc Type Hearing Aid Model U-Impulse Sp

  Class I

  FDA 510(k) K880286 Active Cleared 23 Feb 1988

• Tricon-M Total Knee System

  Class II

  FDA 510(k) K884824 Active Cleared 21 Nov 1989

• Orthopaedic Cable System

  Class II

  FDA 510(k) K842977 Active Cleared 26 Oct 1984

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