BIO-MODULAR SHOULDER SYSTEM
- Primary DI
- 00880304010826
- Brand
- BIO-MODULAR SHOULDER SYSTEM
- Company
- Biomet Orthopedics, LLC
- Model
- 113853
- Catalog number
- 113853
- 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 |
|---|---|
| HSD | PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
| MBF | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED |
| MDF | DNA-PROBE, REAGENTS, COCCIDIOIDES IMMITIS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HSD | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | Orthopedic | 2 |
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| MBF | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented | Orthopedic | 2 |
| MDF | Dna-Probe, Reagents, Coccidioides Immitis | Microbiology | 2 |
Premarket Submissions#
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304010826 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304010826 | 00880304010826 | 880304010826 | 0880304010826 |
GMDN Terms#
| Term | Definition |
|---|---|
| Shoulder glenoid fossa prosthesis, prefabricated | An implantable, prefabricated component of a total shoulder prosthesis (glenoid component) designed to replace or repair the glenoid fossa; it is not a custom-made device. It is cup-like in shape and typically made of polyethylene (PE), but may be made of metal or a combination of PE and metal; it may include fixation devices (e.g., screws) for attachment to the scapula. |
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 |
|---|---|---|---|---|
| 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 |
| 00888480584711 | PRO OSTEON 500R | 5RB040 | 5RB040 | 2015-10-24 |
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| 00887868554407 | Signature™ Comprehensive® | Orthosoft Inc | MBF | 2024-02-09 |
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