What is FDA product code PBI?

For use as a component of a total hip prosthesis in primary and revision patients at high risk of dislocation due to a history of prior dislocation, bone loss, joint or soft tissue laxity, neuromuscular disease, or intraoperative instability, and for whom all other options to constrained acetabular components have been considered.

Orthopedic › ProstheticProsthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive

Sirus

Name: Sirus
Brand: Sirus

Catalogue number SSI004280, listed by Biomet Orthopedics, United States, under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26

5manufacturers in China registered for this device type

1catalogue number

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code PBI
Manufacturer	City	Province	Registered as	Device types
APS Materials Suzhou	Suzhou	Jiangsu	Contract manufacturer	18
Zimmer (Shanghai) Medical International Trading Co., Ltd.	Shanghai	Shanghai	Exporter	106
Zhejiang Biomet Medical Products Co., Ltd.	Jinhua	Zhejiang	Contract manufacturer	74
Shanghai JPY ION-Tech Co., Ltd.	Shanghai	Shanghai	Contract manufacturer	70
Changzhou Biomet Medical Devices Co., Ltd.	Changzhou	Jiangsu	Contract manufacturer	54

Record

Regulatory record for Sirus
Listed by	Biomet Orthopedics, United States
FDA product code	PBI
Device type	Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive
Device class	Class 2
Regulation	21 CFR 888.3310
510(k)	K130610
Record published	2018-07-26
Record revised	2025-05-30 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Sterilisation	Moist Heat or Steam Sterilization
Prescription	Prescription only
Label carries	lot or batch number

Catalogue Numbers

Catalogue numbers for Sirus
Catalogue number	Size	Status
SSI004280		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
G7®	Biomet Orthopedics	45
G7 Acetabular Liner	Biomet Orthopedics	37
Arcos® One-Piece Revision System	Biomet Orthopedics	17
G7® Acetabular System	Biomet Orthopedics	13
G7 Osseoti Acetabular Shell	Biomet Orthopedics	8
Sirius®	Biomet Orthopedics	6
G7® Revision Acetabular System	Zimmer, Inc.	5
G7 Provisional Neutral Liner	Biomet Orthopedics	4
Echo BI-Metric Microplasty HIP Stem	Biomet Orthopedics	4
G7® Freedom® Vivacit-E®	Zimmer, Inc.	4
Sirius HIP System	Biomet Orthopedics	3
G7 Type 12 / 14 Provisional Head	Biomet Orthopedics	3

Showing 12 of 34. All products under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Sirus
Recalled by	Identified by	Initiated	FDA class	Root cause	Reason	Quantity	Closed
Biomet, Inc.	510(k) number	2014-12-02	Class II	Mixed-up of materials/components	After receiving a complaint, Biomet Orthopedic Inc., conducted an investigation which determined that the following parts were mixed up prior to packaging and shipment: Sirius Polish Cemented Stem 34B Catalog Number: 51-199333, Lot Number	9	2015-10-27
Biomet, Inc.	510(k) number	2014-12-02	Class II	Mixed-up of materials/components	After receiving a complaint, Biomet Orthopedic Inc., conducted an investigation which determined that the following parts were mixed up prior to packaging and shipment: Sirius Polish Cemented Stem 348 Catalog Number: 51-199333, Lot Number I	8	2015-10-27

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.