Conquest FN

The Conquest FN proximal locking screw is a fixation component used with the system's contoured bone plate. The construct treats displaced or undisplaced intracapsular femoral neck…

Registry build 21.09.26

The Conquest FN proximal locking screw is a fixation component used with the system’s contoured bone plate. The construct treats displaced or undisplaced intracapsular femoral neck fractures. Compatible locking and nonlocking screws secure the plate-and-screw assembly in the proximal femur.

The described implants are made from implant-grade 316L stainless steel and intended for single use. A sterile packaging option uses gamma irradiation. The listed locking screw belongs to the implant range rather than the separate instruments used to insert it.

Listed Item

Conquest FN 8.5MM X 125MM Proximal Locking Screw Stainless Steel 32MM Thread

System Design

The Conquest FN system combines the contoured locking plate with compatible bone screws and incorporates POGO screw technology. The screw provides fixation as part of that construct. Specific screw diameter, length and thread measurements remain configuration choices within the range.

2manufacturers in China registered for this device type
31catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

All of them in Shanghai. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code JDO
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Conquest FN
Listed by Smith & Nephew, Inc., United States
FDA product code JDO
Device type Device, Fixation, Proximal Femoral, Implant
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K152686
Record published 2016-03-30
Record revised 2024-02-19 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Conquest FN
Catalogue number Size Status
71179211 In distribution
75808225 In distribution
E0015430-1 In distribution
75808085 In distribution
71179231 In distribution
71179203 In distribution
75807105 In distribution
75807220 In distribution
75807095 In distribution
75808220 In distribution
75807200 In distribution
71179202 In distribution
75807075 In distribution
75807115 In distribution
75807001L In distribution
71179208 In distribution
75808000R In distribution
75807003R In distribution
75808095 In distribution
71179213 In distribution
75808080 In distribution
75808130 In distribution
75808205 In distribution
75808001R In distribution
71179219 In distribution
75808210 In distribution
75808003L In distribution
75808105 In distribution
75808125 In distribution
75807080 In distribution
75807001R In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
BMP Compression HIP Screw Biomet Orthopedics 112
DHS Synthes Gmbh 93
THP™ Hip Fracture Plating System Biomet Orthopedics 74
Percutaneous Compression Plate (Pc.c.p) Orthofix SRL 69
Proform Hip System Globus Medical, Inc. 51
CHS Smith & Nephew, Inc. 26
Large Cannulated Screws Smith & Nephew, Inc. 22
TSP HIP FX Plating SYSTEM4.5MM Cortical NON – Locking Screw Biomet Orthopedics 13
TSP HIP FX Plating SYSTEM4.5MM Cortical Locking Screw Biomet Orthopedics 12
TSP HIP FX Plating SYSTEM7.5MM Telescoping LAG Screw Biomet Orthopedics 6
Dhhs Synthes Gmbh 6
3P Hip System Orthopediatrics, Corp 5

Showing 12 of 112. All products under Device, Fixation, Proximal Femoral, Implant

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213126 2022-09-29
K193029 2020-02-28
K172785 2017-12-22
K152686 2016-03-17
K080434 2008-04-10

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