Corin Bipolar Prosthesis

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

510(k) Number

K925897 ↗

FDA Product Code

KWY

Device Class

Class II

Regulation

21 CFR Part 888.3390

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

• Corin Austin-Moore Prosthesis, Modification

  Class II

  FDA 510(k) K931752 Active Cleared 7 Oct 1994

• Nuffield Total Knee Uhmwpe Tibia (One Piece) Modification

  Class II

  FDA 510(k) K934166 Active Cleared 7 Sep 1994

• Cenator Total Hip System

  Class II

  FDA 510(k) K925866 Active Cleared 23 Sep 1993

• Corin Thompson Prosthesis, Modification

  Class II

  FDA 510(k) K931753 Active Cleared 7 Oct 1994