STAR™
GUDID 00886385019031
Lateral I/M Alignment Assembly
Stryker Trauma SA
Orthopaedic implant aiming/guiding block, reusable| Primary Device ID | 00886385019031 |
| NIH Device Record Key | 89afa8b1-864f-4ac9-8747-8dfb96856af5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STAR™ |
| Version Model Number | 933-0025 |
| Company DUNS | 481999654 |
| Company Name | Stryker Trauma SA |
| 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 | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx | |
| Phone | 1-201-831-5000 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886385019031 [Primary] |
FDA Product Code
| NTG | Prosthesis, Ankle, Uncemented, Non-Constrained |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
[00886385019031]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-06-27 |
On-Brand Devices [STAR™]
| 00886385027074 | Silicone Pin Mat |
| 00886385027067 | STAR Instrumentation Case Base #3 |
| 00886385027050 | STAR Instrumentation Case Base #2 |
| 00886385027005 | Sliding Core, UHMPWE, 14mm REVISION |
| 00886385026992 | Sliding Core, UHMPWE, 13mm REVISION |
| 00886385026985 | Sliding Core, UHMPWE, 12mm REVISION |
| 00886385026978 | Sliding Core, UHMPWE, 11mm REVISION |
| 00886385026961 | Sliding Core, UHMPWE, 10mm |
| 00886385026947 | Sliding Core, UHMPWE, 8mm |
| 00886385026930 | Sliding Core, UHMPWE, 7mm |
| 00886385026923 | Sliding Core, UHMPWE, 6mm |
| 00886385019482 | Trial S.T.A.R. P.E. Core 14mm |
| 00886385019475 | Trial S.T.A.R. P.E. Core 13mm |
| 00886385019468 | Trial S.T.A.R. P.E. Core 12mm |
| 00886385019451 | Trial S.T.A.R. P.E. Core 11mm |
| 00886385019406 | DATUM HOLDER ASSEMBLY |
| 00886385019222 | DATUM HOLDER/DISTRACTOR |
| 00886385019215 | ANGEL WING |
| 00886385019154 | TIBIA BARREL HOLE WEDGE |
| 00886385019130 | TIBIAL EXTRACTOR TOOL ASSEMBLY |
| 00886385019031 | Lateral I/M Alignment Assembly |
| 00886385019024 | PIN PULLER |
| 00886385019000 | GEAR KEY |
| 00886385018980 | Tibial Key Hole Cutter, Blade |
| 00886385018966 | Tibial Key Hole Cutter Assembly |
| 00886385018959 | JOINT SPACE EVALUATOR |
| 00886385018928 | Fixation Pin 6.5 x 62mm |
| 00886385018911 | BARREL HOLE PLATE, XLARGE |
| 00886385018904 | BARREL HOLE PLATE, LARGE |
| 00886385018898 | BARREL HOLE PLATE, MEDIUM |
| 00886385018881 | BARREL HOLE PLATE, SMALL |
| 00886385018874 | BARREL HOLE PLATE, XS |
| 00886385018867 | Alignment Pin, 47mm |
| 00886385018850 | Alignment Pin, 35mm |
| 00886385018812 | Tibial Alignment Rotation Sleeve Assembly |
| 00886385018805 | PIN BLOCK ASSEMBLY, SET SCREW |
| 00886385018775 | PIN BLOCK ASSEMBLY |
| 00886385018751 | Adjustable Slider Block Assembly, DoveTail Lock |
| 00886385018744 | Adjustable Slider Block Assembly, Bolt |
| 00886385018720 | Adjustable Slider Block Assembly |
| 00886385018614 | TALAR CUT GUIDE CAPTIVE SCREW |
| 00886385018607 | Forceps, Star Instrumentation |
| 00886385018591 | Tibial Cut Guide, Captive Screw |
| 00886385018584 | PE Trial, Size 14 |
| 00886385018577 | PE Trial, Size 13 |
| 00886385018560 | PE Trial, Size 12 |
| 00886385018553 | PE Trial, Size 11 |
| 00886385018546 | PE Trial, Size 10 |
| 00886385018539 | PE Trial, Size 9 |
| 00886385018522 | PE Trial, Size 8 |
Trademark Results [STAR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STAR 98753633 not registered Live/Pending |
Tan Kingdom LLC 2024-09-16 |
 STAR 98715412 not registered Live/Pending |
USA Sun Paper INC 2024-08-24 |
 STAR 98708504 not registered Live/Pending |
Pillar of Fire 2024-08-20 |
 STAR 98560141 not registered Live/Pending |
Sensiboo 2024-05-20 |
 STAR 98557727 not registered Live/Pending |
Derek Wisti 2024-05-18 |
 STAR 98533260 not registered Live/Pending |
Huang, Feiling 2024-05-03 |
 STAR 98369646 not registered Live/Pending |
Snyder's-Lance, Inc. 2024-01-22 |
 STAR 98316036 not registered Live/Pending |
Oneal, Millie 2023-12-15 |
 STAR 98223192 not registered Live/Pending |
STARmed Co., Ltd. 2023-10-13 |
 STAR 98164203 not registered Live/Pending |
STAR EV Corporation 2023-09-05 |
 STAR 97659253 not registered Live/Pending |
Star Turbine, Inc. 2022-11-02 |
 STAR 97535148 not registered Live/Pending |
STAR MICRONICS CO., LTD. 2022-08-04 |
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