REVISION Hip
- Primary DI
- 08033390046763
- Brand
- REVISION Hip
- Company
- LIMACORPORATE SPA
- Model
- Trial Neck With Screw
- Catalog number
- 9038.10.200
- Device description
- Trial Neck with Screw h=100mm
- Published
- 2016-05-12
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented | Orthopedic | 2 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | Orthopedic | 2 |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K151739 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08033390046763 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08033390046763 | 08033390046763 | 8033390046763 |
GMDN Terms#
| Term | Definition |
|---|---|
| Femoral stem prosthesis trial | A copy of a final femoral stem prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral head trial prostheses. It is typically made of metal or polymer material and includes trial stems, trial sleeves, and trial necks. This is a reusable device intended to be sterilized prior to use. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 432066322
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 08033390216036 | SMR Shoulder | 1379.5G.030 | 1379.5G.030 | 2026-05-11 |
| 08033390216043 | SMR Shoulder | 1379.5G.120 | 1379.5G.120 | 2026-05-11 |
| 08033390216050 | SMR Shoulder | 1379.5G.124 | 1379.5G.124 | 2026-05-11 |
| 08033390216067 | SMR Shoulder | 1379.5G.320 | 1379.5G.320 | 2026-05-11 |
| 08033390216074 | SMR Shoulder | 1379.5G.322 | 1379.5G.322 | 2026-05-11 |
| 08033390216081 | SMR Shoulder | 1379.5G.324 | 1379.5G.324 | 2026-05-11 |
| 08033390216098 | SMR Shoulder | 1379.5G.330 | 1379.5G.330 | 2026-05-11 |
| 08033390272797 | SMR System | 1375.15.605 | 1375.15.605 | 2026-02-25 |
| 08033390272803 | SMR System | 1375.15.610 | 1375.15.610 | 2026-02-25 |
| 08033390272810 | SMR System | 1375.15.620 | 1375.15.620 | 2026-02-25 |
| 08033390002233 | SMR System | 1362.09.010 | 1362.09.010 | 2026-02-19 |
| 08033390002240 | SMR System | 1362.09.015 | 1362.09.015 | 2026-02-19 |
| 08033390002257 | SMR System | 1362.09.020 | 1362.09.020 | 2026-02-19 |
| 08033390050029 | SMR System | 1362.09.115 | 1362.09.115 | 2026-02-19 |
| 08033390050036 | SMR System | 1362.09.120 | 1362.09.120 | 2026-02-19 |
| 08033390191135 | PRIMA | 1367.09.376 | 1367.09.376 | 2026-02-19 |
| 08033390201971 | PRIMA | 1367.09.200 | 1367.09.200 | 2026-02-19 |
| 08033390202299 | PRIMA | 1367.09.203 | 1367.09.203 | 2026-02-19 |
| 08033390202305 | PRIMA | 1367.09.206 | 1367.09.206 | 2026-02-19 |
| 08033390202312 | PRIMA | 1367.09.270 | 1367.09.270 | 2026-02-19 |
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| 04026575448760 | MobileLink Acetabular Cup System | WALDEMAR LINK GmbH & Co. KG | LZO | 2026-07-09 |
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| 04026575448784 | MobileLink Acetabular Cup System | WALDEMAR LINK GmbH & Co. KG | LZO | 2026-07-09 |
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| 04026575448807 | MobileLink Acetabular Cup System | WALDEMAR LINK GmbH & Co. KG | LZO | 2026-07-09 |
| 04026575448807 | MobileLink Acetabular Cup System | WALDEMAR LINK GmbH & Co. KG | LPH | 2026-07-09 |
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