ATTUNE 151630806
GUDID 10603295048114
ATTUNE KNEE SYSTEM TIBIAL INSERT ROTATING PLATFORM CRUCIATE RETAINING SIZE 8 6mm AOX
DEPUY (IRELAND)
Tibial insert| Primary Device ID | 10603295048114 |
| NIH Device Record Key | 7f28d232-d53f-4968-907c-0b63fb141720 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ATTUNE |
| Version Model Number | 1516-30-806 |
| Catalog Number | 151630806 |
| Company DUNS | 989365556 |
| Company Name | DEPUY (IRELAND) |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10603295048114 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P830055
FDA Product Code
| NJL | Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-12-04 |
| Device Publish Date | 2015-03-24 |
On-Brand Devices [ATTUNE]
| 10603295492023 | ATTUNE KNEE SYSTEM REVISION ADAPTOR TRIAL EXTRACTOR |
| 10603295478614 | ATTUNE KNEE SYSTEM REVISION STEM TRIAL DRIVER BIT |
| 10603295451303 | ATTUNE KNEE SYSTEM REVISION FEMORAL TRIAL EXTRACTOR |
| 10603295440499 | ATTUNE KNEE SYSTEM REVISION FEMORAL SLEEVE TAPER SEPARATOR DRIVER |
| 10603295440482 | ATTUNE KNEE SYSTEM REVISION FEMORAL SLEEVE TAPER SEPARATOR BASE |
| 10603295440451 | ATTUNE KNEE SYSTEM REVISION STEM TRIAL AND STABILIZER EXTRACTOR |
| 10603295440390 | ATTUNE KNEE SYSTEM REVISION FEMORAL SLEEVE SEPARATOR PUSH ROD |
| 10603295438700 | ATTUNE KNEE SYSTEM REVISION TIBIAL BASE TRIAL EXTRACTOR |
| 10603295131021 | ATTUNE TRIAL EXTRACTOR |
| 10603295130215 | ATTUNE FEMORAL INTRODUCER |
| 10603295482017 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 24MM |
| 10603295482000 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 20MM |
| 10603295481997 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 18MM |
| 10603295481980 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 14MM |
| 10603295481973 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 12MM |
| 10603295481966 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 10MM |
| 10603295481959 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 8MM |
| 10603295481942 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 6MM |
| 10603295477310 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 26MM |
| 10603295477303 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 24MM |
| 10603295477297 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 22MM |
| 10603295477280 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 20MM |
| 10603295477273 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 18MM |
| 10603295477266 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 16MM |
| 10603295477259 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 14MM |
| 10603295477242 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 12MM |
| 10603295477235 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 10MM |
| 10603295477228 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 8MM |
| 10603295477211 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 10 6MM |
| 10603295477204 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 26MM |
| 10603295477129 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 22MM |
| 10603295477112 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 9 16MM |
| 10603295476009 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 8MM |
| 10603295475996 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 6MM |
| 10603295475989 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 14MM |
| 10603295475972 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 12MM |
| 10603295475965 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 10MM |
| 10603295475804 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 22MM |
| 10603295475798 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 20MM |
| 10603295475781 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 18MM |
| 10603295475774 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 16MM |
| 10603295475767 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 14MM |
| 10603295475750 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 8MM |
| 10603295475743 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 6MM |
| 10603295475736 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 12MM |
| 10603295475729 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 2 10MM |
| 10603295475712 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 26MM |
| 10603295475705 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 24MM |
| 10603295475699 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 22MM |
| 10603295475682 | ATTUNE KNEE SYSTEM REVISION RP INSERT TRIAL SIZE 1 20MM |
Trademark Results [ATTUNE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ATTUNE 98465065 not registered Live/Pending |
Stoic Software 2024-03-24 |
 ATTUNE 98430041 not registered Live/Pending |
LPRG-IP, LLC 2024-03-01 |
 ATTUNE 98425135 not registered Live/Pending |
Bausch & Lomb Incorporated 2024-02-28 |
 ATTUNE 98349229 not registered Live/Pending |
Lendsmart, Inc. 2024-01-09 |
 ATTUNE 98283965 not registered Live/Pending |
Acacia Health Partners 2023-11-24 |
 ATTUNE 97886848 not registered Live/Pending |
Wells Fargo & Company 2023-04-13 |
 ATTUNE 97819473 not registered Live/Pending |
Somavedic Technologies, Inc. 2023-03-02 |
 ATTUNE 97789483 not registered Live/Pending |
Protocol Technologies, Inc. 2023-02-10 |
 ATTUNE 97740723 not registered Live/Pending |
Mannington Mills, Inc. 2023-01-04 |
 ATTUNE 97665205 not registered Live/Pending |
Oerth Bio, LLC 2022-11-07 |
 ATTUNE 97590831 not registered Live/Pending |
Standard Fiber, LLC 2022-09-14 |
 ATTUNE 97263582 not registered Live/Pending |
Senseware, Inc. 2022-02-11 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.