Arthopor-Acetabular Component

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844050 ↗

FDA Product Code

JDI

Device Class

Class II

Regulation

21 CFR Part 888.3350

Advisory Committee

Orthopedic

FDA Decision

SN

• S-ROM Total Hip Replacement System

  Class II

  FDA 510(k) K920739 Active Cleared 24 Nov 1992

• S-ROM ZTT Acetabular Cup-Apical Hole Plug

  Class III

  FDA 510(k) K931676 Active Cleared 18 May 1994

• S-Rom Femoral Hip Stem - Size 14 X 8

  Class II

  FDA 510(k) K954935 Active Cleared 22 Jan 1996

• Knee Prothesis

  Class II

  FDA 510(k) K941769 Active Cleared 1 Feb 1995

• Src Total Knee

  Not classified

  FDA 510(k) K841022 Active Cleared 25 Jun 1984

• S-Rom Opc (One-Piece Cemented) II Femoral Hip Prosthesis

  Class II

  FDA 510(k) K951084 Active Cleared 31 May 1995

See all devices from Joint Medical Products Corp. →

• What is the Arthopor-Acetabular Component used for?

  The Arthopor-Acetabular Component is an orthopedic device designed to replace the acetabulum, which is the socket portion of the hip joint, primarily used in hip replacement surgeries.

• How is the Arthopor-Acetabular Component supplied?

  The device is supplied by Joint Medical Products Corp., though the specific packaging or sterilization details are not provided in the available information.

• What regulatory clearance has the Arthopor-Acetabular Component received?

  The device has received FDA 510(k) clearance with number K844050, determined to be substantially equivalent for some indications as reviewed by the Orthopedic advisory committee.

• Is the Arthopor-Acetabular Component reusable or single-use?

  The available information does not specify whether the device is designed for single-use or multiple uses, as this detail is not included in the provided data.