Avanta Orthopaedics Trapezium Implant

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K965204 ↗

FDA Product Code

KYI

Device Class

Class II

Regulation

21 CFR Part 888.3770

Advisory Committee

Orthopedic

FDA Decision

SN

• Avanta Orthopaedics Trapezial Implant

  Class II

  FDA 510(k) K964381 Active Cleared 22 Jan 1997

• K'fix

  Class II

  FDA 510(k) K010847 Active Cleared 19 Jun 2001

• External Fixation

  Class II

  FDA 510(k) K981716 Active Cleared 17 Jul 1998

• Avanta Orthopaedics Tendon Spacer

  Class II

  FDA 510(k) K964359 Active Cleared 25 Mar 1997

• Finger Joint Prosthesis

  Class II

  FDA 510(k) K013629 Active Cleared 25 Jan 2002

• Distal Radius Fracture Fixation Plate

  Class II

  FDA 510(k) K981715 Active Cleared 29 Jul 1998

See all devices from Avanta Orthopaedics, Inc. →