510(k) Report

FDA applicant

Centerplus Orthopedics, Inc.

Austin, TX2 decisions2003–20038 recalls

FDA records 2 decisions for Centerplus Orthopedics, Inc. (Austin, TX) in 2003: 2 510(k) clearances. Most are in product codes KWS (Prosthesis, Shoulder, Semi-Constrained…) and JWH (Prosthesis, Knee, Patellofemorotibial…). Its devices cite 3 predicates, 0 of them its own earlier devices. 8 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Centerplus Orthopedics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Centerplus Orthopedics, Inc. since 2007.

Recalls per year

3in 2012

2008: 12009: 42012: 3
2007high 4 (2009) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Centerplus Orthopedics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1decision
  • JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 12 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K030259Amatomical Shoulder with Removable HeadCenterplus Orthopedics, Inc. · 20039cite it
  • K023528Natural-Knee II Cemented Modular Tibial BaseplateCenterplus Orthopedics, Inc. · 20033cite it

What has FDA decided for it lately?

  • K030259Amatomical Shoulder with Removable HeadCenterplus Orthopedics, Inc. · 20033 recalls
  • K023528Natural-Knee II Cemented Modular Tibial BaseplateCenterplus Orthopedics, Inc. · 20035 recalls

All 2 as Centerplus Orthopedics, Inc. →

What has been recalled?

8 recalls linked to its devices; the latest:

  • K030259Anatomical Shoulder" Humeral stemSep 4, 2012Class II
  • K030259Anatomical Shoulder" Ball taper for humeral stemSep 4, 2012Class II
  • K030259Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder Fracture…Sep 4, 2012Class II
  • K023528Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 0, TIB…Mar 18, 2009
  • K023528Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 0, TIB B/PL…Mar 18, 2009
  • K023528Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 00, for…Mar 18, 2009