Legend Acetabular Shell

Legend Acetabular Shell is a one-piece hemispherical implant for uncemented total hip replacement. Press-fit contact with the prepared acetabulum provides fixation. The shell’s outer…

Registry build 21.09.26

Legend Acetabular Shell is a one-piece hemispherical implant for uncemented total hip replacement. Press-fit contact with the prepared acetabulum provides fixation. The shell’s outer surface has a sintered porous commercially pure titanium coating.

The shell body is Ti-6Al-4V ELI titanium alloy. Its inner locking surface accepts compatible Legend or Escalade liners made from extensively cross-linked polyethylene. The metal shell and polymer liner provide separate structural and bearing components.

Listed Item

Three Hole, 52 mm

Additional Components and Configurations

The shell is also designed for use with cancellous bone screws and apical plugs. Shell size and hole configuration vary across the family; the filed three-hole, 52 mm shell is one option. The shell is intended for single use with uncemented press-fit fixation.

14manufacturers in China registered for this device type
36catalogue numbers in this listing
13510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LPH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Record

Regulatory record for Legend Acetabular Shell
Listed by Ortho Development Corp., United States
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K242833
Record published 2024-10-22
Record revised 2020-09-09 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Outer diameter 42 to 70 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Legend Acetabular Shell
Catalogue number Size Status
170-0458/A Outer Diameter 58 mm In distribution
170-0552/A Outer Diameter 52 mm In distribution
170-0558 Outer Diameter 58 mm In distribution
170-0544 Outer Diameter 44 mm In distribution
170-0466 Outer Diameter 66 mm In distribution
170-0450/A Outer Diameter 50 mm In distribution
170-0454/A Outer Diameter 54 mm In distribution
170-0562 Outer Diameter 62 mm In distribution
170-0668 Outer Diameter 68 mm In distribution
170-0470 Outer Diameter 70 mm In distribution
170-0560/A Outer Diameter 60 mm In distribution
170-0446/A Outer Diameter 46 mm In distribution
170-0470/A Outer Diameter 70 mm In distribution
170-0658 Outer Diameter 58 mm In distribution
170-0570 Outer Diameter 70 mm In distribution
170-0450 Outer Diameter 50 mm In distribution
170-0460/A Outer Diameter 60 mm In distribution
170-0652 Outer Diameter 52 mm In distribution
170-0560 Outer Diameter 60 mm In distribution
170-0656 Outer Diameter 56 mm In distribution
170-0660 Outer Diameter 60 mm In distribution
170-0552 Outer Diameter 52 mm In distribution
170-0452 Outer Diameter 52 mm In distribution
170-0662 Outer Diameter 62 mm In distribution
170-0554/A Outer Diameter 54 mm In distribution
170-0644 Outer Diameter 44 mm In distribution
170-0464/A Outer Diameter 64 mm In distribution
170-0562/A Outer Diameter 62 mm In distribution
170-0462/A Outer Diameter 62 mm In distribution
170-0462 Outer Diameter 62 mm In distribution
170-0442/A Outer Diameter 42 mm In distribution
170-0566/A Outer Diameter 66 mm In distribution
170-0650 Outer Diameter 50 mm In distribution
170-0456 Outer Diameter 56 mm In distribution
170-0654 Outer Diameter 54 mm In distribution
170-0670 Outer Diameter 70 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Initia Total Hip System Kyocera Medical Technologies, Inc. 1,000
DJO Surgical Encore Medical, L.P. 624
Pinnacle Depuy Orthopaedics, Inc. 613
Trilogy® Longevity® Zimmer, Inc. 564
Instrument Howmedica Osteonics Corp 369
InSitu Hip System Nextstep Arthropedix 368
Trilogy® Zimmer, Inc. 359
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 298
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Zimmer, Inc. 286
Bencox Hip System Corentec Co., Ltd. 286
OrthoMedFlex Orthomedflex LLC 257
Sterizo Total Hip System CPM Medical Consultants, LLC. 240

Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242833 2024-10-11
K173951 2018-05-30
K161080 2016-05-17
K141001 2014-07-30
K132697 2014-06-20
K133386 2014-03-11
K131022 2013-10-16
K103384 2011-03-16
K062775 2007-01-16
K053293 2006-02-16
K042565 2005-04-11
K000321 2000-04-10
K960660 1996-05-08

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880025 1991-12-04 AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS Depuy Intl., Ltd.
P880076 1991-06-17 WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS Dow Corning Wright
P850061 1991-03-08 BIAS(R) FIBER METAL TOTAL HIP SYSTEM Zimmer, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer