ORTHOMATCH 71436308
GUDID 00885556497500
ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 4 RT
Smith & Nephew, Inc.
Knee tibia prosthesis trial| Primary Device ID | 00885556497500 |
| NIH Device Record Key | 178b9e22-f865-4a42-87e2-21f66114e581 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ORTHOMATCH |
| Version Model Number | 71436308 |
| Catalog Number | 71436308 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556497500 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K142807
FDA Product Code
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
[00885556497500]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2015-08-30 |
On-Brand Devices [ORTHOMATCH]
| 00885556707289 | ORTHOMATCH GII TIBIAL PREP & TRIALS TRAY SZ 1-6 |
| 00885556659823 | ORTHOMATCH FEMORAL SIZER POSTERIOR REF |
| 00885556659816 | ORTHOMATCH FEMORAL SIZER ANTERIOR REF |
| 00885556626108 | GII PLASTIC FEM TRIAL PANEL 7-8 |
| 00885556625910 | GII PLASTIC REAMTHRU FEM TRL SZ 8 RT |
| 00885556625903 | GII PLASTIC REAMTHRU FEM TRL SZ 8 LT |
| 00885556625897 | GII PLASTIC REAMTHRU FEM TRL SZ 7 RT |
| 00885556625880 | GII PLASTIC REAMTHRU FEM TRL SZ 7 LT |
| 00885556625873 | GII PLASTIC REAMTHRU FEM TRL SZ 6 RT |
| 00885556625866 | GII PLASTIC REAMTHRU FEM TRL SZ 6 LT |
| 00885556625859 | GII PLASTIC REAMTHRU FEM TRL SZ 5 RT |
| 00885556625842 | GII PLASTIC REAMTHRU FEM TRL SZ 5 LT |
| 00885556625835 | GII PLASTIC REAMTHRU FEM TRL SZ 4 RT |
| 00885556625828 | GII PLASTIC REAMTHRU FEM TRL SZ 4 LT |
| 00885556625811 | GII PLASTIC REAMTHRU FEM TRL SZ 3 RT |
| 00885556625804 | GII PLASTIC REAMTHRU FEM TRL SZ 3 LT |
| 00885556625798 | GII PLASTIC REAMTHRU FEM TRL SZ 2 RT |
| 00885556625781 | GII PLASTIC REAMTHRU FEM TRL SZ 2 LT |
| 00885556625774 | GII PLASTIC REAMTHRU FEM TRL SZ 1 RT |
| 00885556625767 | GII PLASTIC REAMTHRU FEM TRL SZ 1 LT |
| 00885556625354 | GII FEMORAL TRIALS L TRAY PANEL SZ 1-6 |
| 00885556622087 | ORTHOMATCH CR IMPLANT IMPACTOR |
| 00885556622056 | ORTHOMATCH GII TRAPEZOIDAL SPACER |
| 00885556618189 | ORTHOMATCH MODULAR CR LUG PUNCH |
| 00885556583791 | ORTHOMATCH MOD FEMORAL TRIAL IMPACTOR |
| 00885556583784 | ORTHOMATCH MOD PS FEM IMPLANT IMPACTOR |
| 00885556583777 | ORTHOMATCH TIB BASE PLATE ALIGN BULLET |
| 00885556583760 | ORTHOMATCH EM ALIGNMENT DROP ROD GUIDE |
| 00885556583753 | ORTHOMATCH TIB CUT BLOCK 3 DEG CONNECTOR |
| 00885556583746 | ORTHOMATCH FEMORAL A/P SIZER |
| 00885556583739 | ORTHOMATCH DCF ALIGNMENT GUIDE |
| 00885556582916 | ORTHOMATCH ANTR REF A/P TRSLTN GUIDE |
| 00885556581346 | ORTHOMATCH PSTR REF A/P TRSLTN GUIDE |
| 00885556531785 | ORTHOMATCH MODULAR BOX CHISEL |
| 00885556531761 | ORTHOMATCH MODLR PS FEM IMPLANT IMPACTOR |
| 00885556498101 | ORTHOMATCH MODULAR FIN PUNCH SZ 7-8 |
| 00885556498057 | ORTHOMATCH MODULAR FIN PUNCH SZ 5-6 |
| 00885556498002 | ORTHOMATCH MODULAR FIN PUNCH SZ 3-4 |
| 00885556497951 | ORTHOMATCH MODULAR FIN PUNCH SZ 1-2 |
| 00885556497906 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 8 RT |
| 00885556497852 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 8 LT |
| 00885556497807 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 7 RT |
| 00885556497753 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 7 LT |
| 00885556497708 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 6 RT |
| 00885556497654 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 6 LT |
| 00885556497609 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 5 RT |
| 00885556497555 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 5 LT |
| 00885556497500 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 4 RT |
| 00885556497456 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 4 LT |
| 00885556497401 | ORTHOMATCH STEMLESS TIBIAL TRIAL SZ 3 RT |
Trademark Results [ORTHOMATCH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ORTHOMATCH 97174571 not registered Live/Pending |
Smith & Nephew, Inc. 2021-12-16 |
 ORTHOMATCH 88023129 not registered Live/Pending |
Smith & Nephew, Inc. 2018-07-02 |
 ORTHOMATCH 86450650 not registered Dead/Abandoned |
Smith & Nephew, Inc. 2014-11-11 |
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