FDA.reportPublic FDA data

b-ONE™ Primary Acetabular System

Primary DI
00843575100207
Brand
b-ONE™ Primary Acetabular System
Company
B-ONE ORTHO, CORP.
Model
881906158J
Catalog number
881906158J
Device description
SHELL TRIAL, 58MM OUTER DIAMETER, LINER SIZE J
Published
2019-03-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00843575100207PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00843575100207008435751002078435751002070843575100207

GMDN Terms#

Term, Definition table
TermDefinition
Acetabulum prosthesis trial, reusableA copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically made of metal or polymer material and may be designed in the form of cages, shells, augments, or inserts. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
081315444
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00843575127143MOBIO™ Total Knee System882133110988213311092026-03-06
00843575127150MOBIO™ Total Knee System882133111088213311102026-03-06
00843575127167MOBIO™ Total Knee System882133111188213311112026-03-06
00843575127174MOBIO™ Total Knee System882133111388213311132026-03-06
00843575127181MOBIO™ Total Knee System882133111688213311162026-03-06
00843575127198MOBIO™ Total Knee System882133111988213311192026-03-06
00843575127204MOBIO™ Total Knee System882133112288213311222026-03-06
00843575127211MOBIO™ Total Knee System882133112588213311252026-03-06
00843575127228MOBIO™ Total Knee System882133130988213313092026-03-06
00843575127235MOBIO™ Total Knee System882133131088213313102026-03-06
00843575127242MOBIO™ Total Knee System882133131188213313112026-03-06
00843575127259MOBIO™ Total Knee System882133131388213313132026-03-06
00843575127266MOBIO™ Total Knee System882133131688213313162026-03-06
00843575127273MOBIO™ Total Knee System882133131988213313192026-03-06
00843575127280MOBIO™ Total Knee System882133132288213313222026-03-06
00843575127297MOBIO™ Total Knee System882133132588213313252026-03-06
00843575127303MOBIO™ Total Knee System882133150988213315092026-03-06
00843575127310MOBIO™ Total Knee System882133151088213315102026-03-06
00843575127327MOBIO™ Total Knee System882133151188213315112026-03-06
00843575127334MOBIO™ Total Knee System882133151388213315132026-03-06

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10885862653970AlteonExactech, Inc.MEH2026-05-26
10885862653987AlteonExactech, Inc.MEH2026-05-26