Vitoss
- Primary DI
- 00808232000108
- Brand
- Vitoss
- Company
- Stryker Corporation
- Model
- 2102-0033
- Catalog number
- 2102-0033
- Device description
- Bone Graft Substitute, 1-4mm Morsels Filled Canister, Beta-Tricalcium Phosphate
- Published
- 2015-09-24
- 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 |
|---|---|
| MQV | FILLER, BONE VOID, CALCIUM COMPOUND |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MQV | Filler, Bone Void, Calcium Compound | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K032130 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00808232000108 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00808232000108 | 00808232000108 | 808232000108 | 0808232000108 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone matrix implant, synthetic | A sterile bioabsorbable device made of synthetic material intended to be implanted into the body to provide osteoconductive bone-tissue scaffolds, and sometimes osteovascularization, to replace bone lost through trauma, surgery, or pathological conditions (e.g., osteoporosis). It may be made of ceramics (e.g., tricalcium phosphate or hydroxyapatite), bioactive glasses/minerals/metals (e.g., strontium), or bioabsorbable polymers. It is used to fill cystic defects, repair fractures, and/or extend autogenous bone grafts and is typically provided as cancellous blocks, chips, or granules of varying sizes, or mouldable/fluid materials. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Ambient |
| Special Storage Condition, Specify | 0 | 0 | Do Not Expose to Extreme Heat |
| Special Storage Condition, Specify | 0 | 0 | Do Not Freeze |
| Storage Environment Temperature | 0 | 25 Degrees Celsius | |
| Storage Environment Temperature | 15 Degrees Celsius | 25 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(610)640-1775 | spacustserv@stryker.com |
Regulatory Flags#
- DUNS number
- 149183167
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04546540434364 | SpinePlex | 0406202000 | 0406-202-000 | 2016-06-30 |
| 07613154599097 | NA | 5920000201 | 5920-000-201 | 2016-09-23 |
| 07613154599103 | NA | 5920000202 | 5920-000-202 | 2018-09-24 |
| 07613154599110 | NA | 5920000203 | 5920-000-203 | 2018-09-24 |
| 07613154599134 | NA | 5920000205 | 5920-000-205 | 2018-09-24 |
| 07613154599141 | NA | 5920000206 | 5920-000-206 | 2018-09-24 |
| 07613154599158 | NA | 5920000207 | 5920-000-207 | 2018-09-24 |
| 07613154599165 | NA | 5920000208 | 5920-000-208 | 2018-09-24 |
| 07613154599172 | NA | 5920000209 | 5920-000-209 | 2018-09-24 |
| 07613154599189 | NA | 5920000301 | 5920-000-301 | 2018-09-24 |
| 07613154599196 | NA | 5920000302 | 5920-000-302 | 2018-09-24 |
| 07613154599202 | NA | 5920000303 | 5920-000-303 | 2018-09-24 |
| 07613154599219 | NA | 5920000304 | 5920-000-304 | 2018-09-24 |
| 07613154599226 | NA | 5920000305 | 5920-000-305 | 2018-09-24 |
| 07613154599233 | NA | 5920000306 | 5920-000-306 | 2018-09-24 |
| 07613154599240 | NA | 5920000307 | 5920-000-307 | 2018-09-24 |
| 07613154615513 | NA | 5920000309 | 5920-000-309 | 2018-09-24 |
| 07613252254430 | VertaPlex | 0406622000 | 0406-622-000 | 2016-09-23 |
| 07613327141771 | SpinePlex | 0406222000 | 0406222000 | 2016-09-23 |
| 07613327141788 | SpinePlex | 0406202010 | 0406-202-010 | 2016-09-23 |
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