Vitoss
- Primary DI
- 00808232000382
- Brand
- Vitoss
- Company
- Stryker Corporation
- Model
- 2102-1310
- Catalog number
- 2102-1310
- Device description
- Bone Graft Substitute, Foam Flow, Beta-Tricalcium Phosphate and Type I Bovine Collagen
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- Not 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 |
|---|---|
| K032288 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00808232000382 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00808232000382 | 00808232000382 | 808232000382 | 0808232000382 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone matrix implant, composite | A sterile bioabsorbable device made of synthetic bone substitute materials (e.g., ceramics such as tricalcium phosphate or hydroxyapatite) combined with bone growth factors (e.g., bovine collagen) implanted into the body to provide osteoconductive bone-tissue scaffolds to replace bone lost through trauma, surgery, or pathological conditions (e.g., osteoporosis). It is used to fill cystic defects, repair fractures, and/or extend autogenous bone grafts. It is typically provided as cancellous blocks, chips, or granules of varying sizes, or mouldable 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 | 15 Degrees Celsius | 25 Degrees Celsius | |
| Storage Environment Temperature | 20 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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