Partnership Revision Femoral Stems

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

510(k) Number

K972893 ↗

FDA Product Code

LZO

Device Class

Class II

Regulation

21 CFR Part 888.3353

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

• Howmedica(R) Fully Threaded Screws

  Class II

  FDA 510(k) K974720 Active Cleared 13 Mar 1998

• Alta Femoral Intramedullary Rods/Cfx Rods Modification

  Class II

  FDA 510(k) K935295 Active Cleared 11 Oct 1994

• Naso-Gard Nasogastric Tube Holder

  Class II

  FDA 510(k) K801511 Active Cleared 28 Jul 1980

• Class of Casting Alloys Type III or Alt

  Class II

  FDA 510(k) K820434 Active Cleared 11 Mar 1982

• Howmedica Zirconia Ceramic Femoral Head

  Class II

  FDA 510(k) K945090 Active Cleared 19 Jan 1995

• Extended Balljoint Grip

  Class II

  FDA 510(k) K802723 Active Cleared 19 Nov 1980

See all devices from Howmedica Corp. →

• What are Partnership Revision Femoral Stems used for?

  Partnership Revision Femoral Stems are titanium implants designed for use in both primary and revision total hip arthroplasty procedures. They are press-fit into the proximal femur and do not achieve biological ingrowth fixation.

• What components are compatible with these femoral stems?

  These stems are designed to be used with Howmedica V40 femoral heads, unipolar/bipolar components, and acetabular components to complete the total hip arthroplasty system.

• What is the regulatory status of these implants?

  The device received FDA 510(k) clearance with K972893 on November 3, 1997, and is classified under product code LZO. It was determined to be substantially equivalent through the traditional clearance process.

• What is the fixation mechanism of these stems?

  Partnership Revision Femoral Stems utilize a press-fit fixation method into the proximal femur. They do not achieve biological ingrowth fixation, relying instead on the mechanical press-fit stability.