Compress® Device
- Primary DI
- 00880304508941
- Brand
- Compress® Device
- Company
- Biomet Orthopedics, LLC
- Model
- 178351
- Catalog number
- 178351
- Published
- 2015-10-24
- 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 |
|---|---|
| JDC | PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
| KRO | PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
| MBF | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED |
| MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JDC | Prosthesis, Elbow, Constrained, Cemented | Orthopedic | 2 |
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | Orthopedic | 2 |
| KRO | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented | Orthopedic | 2 |
| KWZ | Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer | 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 |
| MBF | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented | Orthopedic | 2 |
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K101475 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304508941 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304508941 | 00880304508941 | 880304508941 | 0880304508941 |
GMDN Terms#
| Term | Definition |
|---|---|
| Body femoral/tibial extension stem, coated | A sterile implantable device intended to provide an extension of, or coupling with, other components of a modular femoral/tibial prosthesis in the medullary canal to compensate for bone loss during revision arthroplasty or bone resection. The device is a solid/dense body 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. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887868494758 | Vanguard® Instruments | 32-486259 | 32-486259 | 2022-05-25 |
| 00888480584162 | PRO OSTEON 200 | 2B040 | 2B040 | 2015-10-24 |
| 00888480584179 | PRO OSTEON 200 | 2B045 | 2B045 | 2015-10-24 |
| 00888480584186 | PRO OSTEON 200 | 2B075 | 2B075 | 2015-10-24 |
| 00888480584247 | PRO OSTEON 200 | 2G02 | 2G02 | 2015-10-24 |
| 00888480584254 | PRO OSTEON 200 | 2G05 | 2G05 | 2015-10-24 |
| 00888480584339 | PRO OSTEON 200R | 2RG005 | 2RG005 | 2015-10-24 |
| 00888480584346 | PRO OSTEON 200R | 2RG02 | 2RG02 | 2015-10-24 |
| 00888480584353 | PRO OSTEON 200R | 2RG05 | 2RG05 | 2015-10-24 |
| 00888480584360 | PRO OSTEON 200R | 2RG15 | 2RG15 | 2015-10-24 |
| 00888480584476 | PRO OSTEON 500 | 5B040 | 5B040 | 2015-10-24 |
| 00888480584483 | PRO OSTEON 500 | 5B075 | 5B075 | 2015-10-24 |
| 00888480584490 | PRO OSTEON 500 | 5B100 | 5B100 | 2015-10-24 |
| 00888480584575 | PRO OSTEON 500 | 5G05 | 5G05 | 2015-10-24 |
| 00888480584582 | PRO OSTEON 500 | 5G10 | 5G10 | 2015-10-24 |
| 00888480584599 | PRO OSTEON 500 | 5G15 | 5G15 | 2015-10-24 |
| 00888480584629 | PRO OSTEON 500 | 5G30 | 5G30 | 2015-10-24 |
| 00888480584681 | PRO OSTEON 500R | 5RB010 | 5RB010 | 2015-10-24 |
| 00888480584698 | PRO OSTEON 500R | 5RB014 | 5RB014 | 2015-10-24 |
| 00888480584704 | PRO OSTEON 500R | 5RB024 | 5RB024 | 2015-10-24 |
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