Rotaglide+ Modular Knee System with Fixed Meniscus
- Primary DI
- 05055196975248
- Brand
- Rotaglide+ Modular Knee System with Fixed Meniscus
- Company
- CORIN LTD
- Model
- 102.133
- Catalog number
- 102.133
- Device description
- TIBIA BASEPLATE WITH LATCH
- Published
- 2016-08-17
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K000232 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05055196975248 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05055196975248 | 05055196975248 | 5055196975248 |
GMDN Terms#
| Term | Definition |
|---|---|
| Uncoated knee tibia prosthesis, metallic | An implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with an insert and/or the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement. |
Sterilization Methods#
| Method |
|---|
| Radiation Sterilization |
Contacts#
| Phone | |
|---|---|
| +441285659866 | rachel.king@coringroup.com |
| +441285659866 | lucinda.gerber@coringroup.com |
Regulatory Flags#
- DUNS number
- 295437313
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Expiration date on label
- true
- Sterilization required before use
- true
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|---|---|---|---|---|
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| 05056139244940 | Apollo Knee | TKR.BB.1403 | 2025-04-07 | |
| 05056139244971 | Apollo Knee | TKR.IN.1600 | 2025-04-07 | |
| 05056139244988 | Apollo Knee | TKR.IN.1700 | 2025-04-07 | |
| 05056139244995 | Apollo Knee | TKR.BB.1700 | 2025-04-07 | |
| 05056139245008 | Apollo Knee | TKR.BB.1701 | 2025-04-07 | |
| 05056139245015 | Apollo Knee | TKR.BB.1702 | 2025-04-07 | |
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| 05056139245145 | Apollo Knee | TKR.IN.1800 | 2025-04-07 | |
| 05056139245176 | Apollo Knee | TKR.BB.1500 | 2025-04-07 | |
| 05056139245718 | Apollo Knee | TKR.IN.1400 | 2025-04-07 | |
| 05056139245770 | Apollo Knee | TKR.BB.1100 | 2025-04-07 | |
| 05056139245787 | Apollo Knee | TKR.BB.1101 | 2025-04-07 | |
| 05056139245794 | Apollo Knee | TKR.BB.1102 | 2025-04-07 | |
| 05056139245800 | Apollo Knee | TKR.BB.1103 | 2025-04-07 | |
| 05056139245817 | Apollo Knee | TKR.BB.1200 | 2025-04-07 |
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