NA
- Primary DI
- 10885862052698
- Brand
- NA
- Company
- Exactech, Inc.
- Model
- 205-75-02
- Catalog number
- 205-75-02
- Device description
- TIBIAL AUG. BLOCK TEMPLATE, SIZE 2
- Published
- 2022-08-18
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
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 |
|---|---|
| K935726 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10885862052698 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10885862052698 | 10885862052698 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 157565946
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10885862094780 | OpteCure | 650-00-01 | 650-00-01 | 2016-07-17 |
| 10885862094797 | OpteCure | 650-00-02 | 650-00-02 | 2016-07-17 |
| 10885862094803 | OpteCure | 650-00-05 | 650-00-05 | 2016-06-17 |
| 10885862094810 | OpteCure | 650-00-10 | 650-00-10 | 2016-07-17 |
| 10885862094827 | Optecure | 650-00-20 | 650-00-20 | 2016-09-19 |
| 10885862094841 | OpteCure+CCC | 652-00-01 | 652-00-01 | 2016-07-17 |
| 10885862094858 | OpteCure+CCC | 652-00-02 | 652-00-02 | 2016-07-17 |
| 10885862094865 | OpteCure+CCC | 652-00-05 | 652-00-05 | 2016-07-17 |
| 10885862094872 | OpteCure+CCC | 652-00-10 | 652-00-10 | 2016-07-17 |
| 10885862094889 | OpteCure+CCC | 652-00-20 | 652-00-20 | 2016-07-17 |
| 10885862095039 | Ossigen | 660-00-20 | 660-00-20 | 2016-07-17 |
| 10885862252593 | Entice +CCC | 692-00-01 | 692-00-01 | 2016-07-17 |
| 10885862252609 | Entice +CCC | 692-00-02 | 692-00-02 | 2016-07-17 |
| 10885862252616 | Entice +CCC | 692-00-05 | 692-00-05 | 2016-07-17 |
| 10885862252623 | Entice +CCC | 692-00-10 | 692-00-10 | 2016-07-17 |
| 10885862252630 | Entice +CCC | 692-00-20 | 692-00-20 | 2016-07-17 |
| 10885862252845 | Entice | 690-00-01 | 690-00-01 | 2016-07-17 |
| 10885862252852 | Entice | 690-00-02 | 690-00-02 | 2016-07-17 |
| 10885862252869 | Entice | 690-00-05 | 690-00-05 | 2016-07-17 |
| 10885862252876 | Entice | 690-00-10 | 690-00-10 | 2016-07-17 |
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