ChronOS
- Primary DI
- H98071000198S0
- Brand
- ChronOS
- Company
- SYNTHES (U.S.A.) LP
- Model
- 710.001.98S
- Catalog number
- 71000198S
- Device description
- CHRONOS(TM) BETA-TCP GRANULES 0.7-1.4MM/0.5CC-STERILE
- Published
- 2015-09-14
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FMF | Syringe, piston |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FMF | Syringe, Piston | General Hospital | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K041350 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10887587060750 | Primary | GS1 | 0 | |
| H98071000198S0 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10887587060750 | 10887587060750 |
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. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 832637081
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10886982249210 | NA | 60.550.040 | 60550040 | 2017-02-20 |
| 10886982239884 | NA | 530.412 | 530412 | 2016-12-31 |
| 10886982192172 | NA | 329.722 | 329722 | 2017-02-20 |
| 10886982192295 | LC-DCP | 329.918 | 329918 | 2017-02-20 |
| 10886982201461 | NA | 398.56 | 39856 | 2017-02-20 |
| 10886982201478 | NA | 398.58 | 39858 | 2017-02-20 |
| 10705034718040 | NA | 03.620.219 | 03620219 | 2018-10-29 |
| 10705034767802 | VentroFix | 304.832 | 304832 | 2016-12-31 |
| 10705034775418 | NA | 389.296 | 389296 | 2016-12-31 |
| 10705034775425 | NA | 389.297 | 389297 | 2016-12-31 |
| 10705034775432 | NA | 389.298 | 389298 | 2016-12-31 |
| 10705034775449 | NA | 389.299 | 389299 | 2016-12-31 |
| 10705034798455 | NA | 690.038 | 690038 | 2016-12-31 |
| 10887587039893 | NA | 338.761 | 338761 | 2016-12-31 |
| 10886982338778 | MAXFRAME | 1100022-01 | 110002201 | 2024-02-05 |
| 10886982338570 | MAXFRAME | 1100011-01 | 110001101 | 2022-04-26 |
| 10886982338587 | MAXFRAME | 1100010-01 | 110001001 | 2022-04-26 |
| 10886982338594 | MAXFRAME | 1100012-01 | 110001201 | 2022-04-26 |
| 10886982338600 | MAXFRAME | 1100007-01 | 110000701 | 2022-04-26 |
| 10886982237217 | NA | 510.161 | 510161 | 2019-02-21 |
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