Stelkast Surpass Acetabular System

No FDA recalls found in the data synced 6 Oct 2026.

Generic Name

Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented

PMA Number

P040051 ↗

FDA Product Code

MRA

Device Class

Class III

Advisory Committee

Orthopedic

FDA Decision

APWD Approval withdrawn

• GENFlex2 Total Knee System - Ultra-Congruent CR Tibial Insert

  Class II

  FDA 510(k) K173875 Active Cleared 19 Jan 2018

• Protract Press Fit Hip Stem

  Class II

  FDA 510(k) K003447 Active Cleared 15 Dec 2000

• Proform Cemented Femoral Component

  Class II

  FDA 510(k) K951083 Active Cleared 22 May 1995

• Dual Taper Wedge Pressed Fit Femoral Component

  Class II

  FDA 510(k) K953268 Active Cleared 17 Jan 1996

• Proven Knee System

  Class II

  FDA 510(k) K000113 Active Cleared 4 Apr 2000

• Stelkast Bipolar System

  Class II

  FDA 510(k) K972961 Active Cleared 4 Nov 1997

See all devices from Stelkast Company →