Legion Revision
- Primary DI
- 00885556734513
- Brand
- Legion Revision
- Company
- Smith & Nephew, Inc.
- Model
- E0016269-13
- Catalog number
- E0016269-13
- Device description
- AP HEMI-DISTAL SHIM - 5MM - SIZE 5-6R
- Published
- 2018-11-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HRY | Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K121393 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00885556734513 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00885556734513 | 00885556734513 | 885556734513 | 0885556734513 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic prosthesis implantation instrument, reusable | A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00885556925690 | NA | ROB30080 | ROB30080 | 2026-06-04 |
| 03596010589101 | JOURNEY | 71422274 | 71422274 | 2015-08-30 |
| 03596010589132 | JOURNEY | 71422277 | 71422277 | 2015-08-30 |
| 03596010000675 | OXINIUM | 71343603 | 71343603 | 2015-08-30 |
| 03596010474148 | OXINIUM | 71342800 | 71342800 | 2015-08-30 |
| 03596010474162 | OXINIUM | 71342804 | 71342804 | 2015-08-30 |
| 03596010474179 | OXINIUM | 71342808 | 71342808 | 2015-08-30 |
| 03596010474209 | OXINIUM | 71343200 | 71343200 | 2015-08-30 |
| 03596010474216 | OXINIUM | 71343203 | 71343203 | 2015-08-30 |
| 03596010474223 | OXINIUM | 71343204 | 71343204 | 2015-08-30 |
| 03596010474230 | OXINIUM | 71343208 | 71343208 | 2015-08-30 |
| 03596010477279 | OXINIUM | 71343600 | 71343600 | 2015-08-30 |
| 03596010477286 | OXINIUM | 71343604 | 71343604 | 2015-08-30 |
| 03596010477293 | OXINIUM | 71343608 | 71343608 | 2015-08-30 |
| 03596010488862 | OXINIUM | 71342200 | 71342200 | 2015-08-30 |
| 03596010544193 | JOURNEY | 71461012 | 71461012 | 2015-08-30 |
| 03596010544209 | JOURNEY | 71461013 | 71461013 | 2015-08-30 |
| 03596010544216 | JOURNEY | 71461014 | 71461014 | 2015-08-30 |
| 03596010544223 | JOURNEY | 71461015 | 71461015 | 2015-08-30 |
| 03596010544230 | JOURNEY | 71461016 | 71461016 | 2015-08-30 |
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