Klassic HD Hooded Acetabular Insert With Xlpe Poly
Hooded Acetabular Insert with XLPE Poly, 32mm head, size 54mm
8manufacturers in China registered for this device type
20catalogue numbers in this listing
2510(k) clearances naming this product code
Who Else Makes It
Concentrated in Shanghai (3), Jiangsu (3), Zhejiang (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| 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 |
| APS Materials Suzhou | Suzhou | Jiangsu | Contract manufacturer | 18 |
| 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 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| Shenzhen Fox Hunting E-commerce Co., Ltd. | Shenzhen | Guangdong | Exporter | 7 |
Record
| Listed by | Total Joint Orthopedics, Inc., United States |
|---|---|
| FDA product code | OQG |
| Device type | Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3358 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer |
| 510(k) | K180929 |
| Record published | 2018-06-12 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Ethylene Oxide |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: The Klassic HD Hip System should be stored in a clean, dry location at room temperature |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 3508.54.032 | 32mm head, size 54mm | In distribution |
| 3508.58.036 | 36mm head, size 58mm | In distribution |
| 3508.62.032 | 32mm head, size 62mm | In distribution |
| 3508.44.028 | 28mm head, size 44mm | In distribution |
| 3508.62.036 | 36mm head, size 62mm | In distribution |
| 3508.50.032 | 32mm head, size 50mm | In distribution |
| 3508.52.036 | 36mm head, size 52mm | In distribution |
| 3508.64.036 | 36mm head, size 64mm | In distribution |
| 3508.46.028 | 28mm head, size 46mm | In distribution |
| 3508.64.032 | 32mm head, size 64mm | In distribution |
| 3508.44.022 | 22mm head, size 44mm | In distribution |
| 3508.56.036 | 36mm head, size 56mm | In distribution |
| 3508.54.036 | 36mm head, size 54mm | In distribution |
| 3508.58.032 | 32mm head, size 58mm | In distribution |
| 3508.60.032 | 32mm head, size 60mm | In distribution |
| 3508.48.032 | 32mm head, size 48mm | In distribution |
| 3508.60.036 | 36mm head, size 60mm | In distribution |
| 3508.46.022 | 22mm head, size 46mm | In distribution |
| 3508.56.032 | 32mm head, size 56mm | In distribution |
| 3508.52.032 | 32mm head, size 52mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| CS2 Acet. Cup Sys. – VitalitE | Shalby Advanced Technologies, Inc. | 169 |
| iTotal® Hip Replacement System | ConforMIS, Inc. | 131 |
| CS2 Acet. Cup Sys. – VitalitE | Consensus Orthopedics, Inc. | 124 |
| DJO Surgical | Encore Medical, L.P. | 99 |
| MobileLink Acetabular Cup System | Waldemar Link GmbH & Co. KG | 68 |
| G7 | Biomet Orthopedics | 54 |
| Vitelene® | Aesculap AG | 52 |
| Conformis Hip System | ConforMIS, Inc. | 51 |
| Onvoy | Globus Medical, Inc. | 48 |
| Ringloc HIP System | Biomet Orthopedics | 35 |
| Novosource Total Hip System | Novosource, LLC | 33 |
| Prime | Microport Orthopedics Inc. | 32 |
Showing 12 of 100. All products under Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K173104 | 2017-10-27 |
| K141972 | 2014-10-09 |
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.