REDAPT
- Primary DI
- 00885556023518
- Brand
- REDAPT
- Company
- Smith & Nephew, Inc.
- Model
- 71354033
- Catalog number
- 71354033
- Device description
- REDAPT MODULAR SLEEVE SMALL SIZE 16-17 STIKTITE WITH HYDROXYAPATITE
- Published
- 2015-08-30
- 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 |
|---|---|
| MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K081124 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00885556023518 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00885556023518 | 00885556023518 | 885556023518 | 0885556023518 |
GMDN Terms#
| Term | Definition |
|---|---|
| Sleeve femoral/tibial extension, coated | A sterile implantable device typically designed to be attached to a revision femoral stem, knee femur prosthesis, femur/tibia shaft prosthesis, or body femoral/tibial extension stem to extend length to make up for bone loss during revision arthroplasty or bone resection. The device is a hollow sleeve made of metal [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel] and is coated with a material (e.g., porous materials, hydroxyapatite) intended to improve fixation and stability by promoting bone ingrowth. Fixation devices for implantation (e.g., screws and bolts) may be included. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00885556819784 | UNI-CP Compression Plate | 286310ND | 286310ND | 2023-10-26 |
| 00885556819791 | UNI-CP Compression Plate | 286312ND | 286312ND | 2023-10-26 |
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| 00885556831892 | Salto Talaris Total Ankle Prosthesis | LJU225T | LJU225T | 2022-12-21 |
| 00885556835333 | Ti6 Internal Fixation System | FS2040 | FS2040 | 2022-12-22 |
| 00885556839034 | Total Foot System 2 | 2833035 | 2833035 | 2022-12-21 |
| 00885556839058 | Total Foot System 2 | 2835010 | 2835010 | 2022-12-21 |
| 00885556839065 | Total Foot System 2 | 2835012 | 2835012 | 2022-12-21 |
| 00885556839096 | Total Foot System 2 | 2835018 | 2835018 | 2022-12-21 |
| 00885556839126 | Total Foot System 2 | 2835024 | 2835024 | 2022-12-21 |
| 00885556839157 | Total Foot System 2 | 2835030 | 2835030 | 2022-12-21 |
| 00885556839164 | Total Foot System 2 | 2835035 | 2835035 | 2022-12-21 |
| 00885556839409 | Total Foot System 2 | 2845120 | 2845120 | 2022-12-21 |
| 00885556841419 | XT Revision Ankle Replacement System | LJV316T | LJV316T | 2022-12-21 |
| 00885556865118 | Universal2 Total Wrist Implant System | 264535 | 264535 | 2023-01-19 |
| 00885556865231 | Universal2 Total Wrist Implant System | 266301 | 266301 | 2023-01-19 |
| 00885556865279 | Universal2 Total Wrist Implant System | 266402 | 266402 | 2023-01-19 |
| 00885556835647 | Ti6 Internal Fixation System | TC2508 | TC2508 | 2022-12-22 |
| 00885556835654 | Ti6 Internal Fixation System | TC2510 | TC2510 | 2022-12-22 |
| 00885556835760 | Ti6 Internal Fixation System | TC3010 | TC3010 | 2022-12-22 |
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