NA
- Primary DI
- H9804496440
- Brand
- NA
- Company
- SYNTHES (U.S.A.) LP
- Model
- 449.644
- Catalog number
- 449644
- Device description
- TI LOCKING RECON PLATE WITH CONDYLAR HEAD/3X16 HOLES/RIGHT
- 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
- false
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| NEI | Prosthesis, condyle, mandibular, temporary |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| NEI | Prosthesis, Condyle, Mandibular, Temporary | Dental | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K990637 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10887587054537 | Primary | GS1 | 0 | |
| H9804496440 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10887587054537 | 10887587054537 |
GMDN Terms#
| Term | Definition |
|---|---|
| Craniofacial fixation plate, non-bioabsorbable | A small, implantable sheet of firm material that is attached with screws to fractured craniofacial bone (including the maxilla and/or mandible), to bridge and stabilize the fracture gap, and shield the site from stress as the bone heals; the material cannot be chemically degraded or absorbed by natural body processes [includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre]. The device may also be used for craniofacial reconstructive procedures (e.g., to treat congenital malformations), endobrow fixation, or craniotomy flap fixation. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705034731650 | NA | 03.820.126 | 03820126 | 2016-12-31 |
| 10705034731667 | NA | 03.820.127 | 03820127 | 2016-12-31 |
| 10705034731674 | NA | 03.820.128 | 03820128 | 2016-12-31 |
| 10705034731681 | NA | 03.820.129 | 03820129 | 2016-12-31 |
| 10705034731759 | NA | 03.820.136 | 03820136 | 2016-12-31 |
| 10705034731766 | NA | 03.820.137 | 03820137 | 2016-12-31 |
| 10705034731896 | PRODISC L | 03.820.201 | 03820201 | 2016-12-31 |
| 10705034731902 | PRODISC L | 03.820.202 | 03820202 | 2016-12-31 |
| 10705034732008 | NA | 03.820.459 | 03820459 | 2016-12-31 |
| 10705034732015 | NA | 03.820.462 | 03820462 | 2016-12-31 |
| 10705034763729 | ProDisc-C | 09.820.025S | 09820025S | 2014-09-08 |
| 10705034763736 | ProDisc-C | 09.820.026S | 09820026S | 2014-09-08 |
| 10705034763750 | ProDisc-C | 09.820.035S | 09820035S | 2014-09-08 |
| 10705034763767 | ProDisc-C | 09.820.036S | 09820036S | 2014-09-08 |
| 10705034763781 | ProDisc-C | 09.820.045S | 09820045S | 2014-09-08 |
| 10705034763798 | ProDisc-C | 09.820.046S | 09820046S | 2014-09-08 |
| 10705034763804 | ProDisc-C | 09.820.047S | 09820047S | 2014-09-08 |
| 10705034763811 | ProDisc-C | 09.820.055S | 09820055S | 2014-09-08 |
| 10705034763828 | ProDisc-C | 09.820.056S | 09820056S | 2014-09-08 |
| 10705034763835 | ProDisc-C | 09.820.057S | 09820057S | 2014-09-08 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 37613327572088 | Universal Mandible AXS | Stryker Leibinger GmbH & Co. KG | NEI | 2023-09-15 |
| 07613327572087 | Universal Mandible AXS | Stryker Leibinger GmbH & Co. KG | NEI | 2023-09-15 |
| 10888118131260 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2021-11-22 |
| 00888118131249 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2021-11-22 |
| 00888118131256 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2021-11-22 |
| 00888118131263 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2021-11-22 |
| 00888118113016 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2018-01-26 |
| 00888118073471 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00888118073488 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00888118073501 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00888118073518 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00888118073532 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00888118073570 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 10888118073492 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 10888118073553 | LEVEL ONE CMF | KLS-Martin L.P. | NEI | 2016-03-24 |
| 00841036009830 | """2.4MM"" LOCKING RECON SYSTEM" | BIOMET MICROFIXATION, INC | NEI | 2015-10-11 |
| 00841036009847 | """2.4MM"" LOCKING RECON SYSTEM" | BIOMET MICROFIXATION, INC | NEI | 2015-10-11 |
| 00841036091507 | """2.4MM"" LOCKING RECON SYSTEM" | BIOMET MICROFIXATION, INC | NEI | 2015-10-11 |
| 34546540373985 | NA | Stryker Leibinger GmbH & Co. KG | NEI | 2015-09-24 |
| 04546540373991 | NA | Stryker Leibinger GmbH & Co. KG | NEI | 2015-09-24 |
| 04546540374004 | NA | Stryker Leibinger GmbH & Co. KG | NEI | 2015-09-24 |
| 10887587016382 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016399 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016405 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016412 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016429 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016436 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587016443 | MatrixMANDIBLE | Synthes GmbH | NEI | 2015-09-14 |
| 10887587054537 | NA | Synthes GmbH | NEI | 2015-09-14 |
| 10887587054544 | NA | Synthes GmbH | NEI | 2015-09-14 |