Duracon 6478-6-445
GUDID 07613327044799
Cobalt Chrome Stem
Howmedica Osteonics Corp.
Knee femur stem prosthesis| Primary Device ID | 07613327044799 |
| NIH Device Record Key | 3265c080-e285-4e42-867d-194d52765e92 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Duracon |
| Version Model Number | 6478-6-445 |
| Catalog Number | 6478-6-445 |
| Company DUNS | 058311945 |
| Company Name | Howmedica Osteonics Corp. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 155 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327044799 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-20 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [Duracon]
| 07613327141283 | Tibial Bearing Insert - CS |
| 07613327101904 | Inset Patella |
| 07613327101867 | Inset Patella |
| 07613327101850 | Asymmetric Patella |
| 07613327050271 | Total Stabilizer Offset Adapter |
| 07613327050264 | Total Stabilizer Offset Adapter |
| 07613327050257 | Total Stabilizer Offset Adapter |
| 07613327050042 | Total Stabilizer Offset Adapter |
| 07613327049701 | Lipped Tibial Insert |
| 07613327049695 | Lipped Tibial Insert |
| 07613327049688 | Lipped Tibial Insert |
| 07613327049671 | Lipped Tibial Insert |
| 07613327049664 | Lipped Tibial Insert |
| 07613327049657 | Lipped Tibial Insert |
| 07613327049640 | Lipped Tibial Insert |
| 07613327049633 | Lipped Tibial Insert |
| 07613327049626 | Lipped Tibial Insert |
| 07613327049619 | Lipped Tibial Insert |
| 07613327049602 | Lipped Tibial Insert |
| 07613327049596 | Lipped Tibial Insert |
| 07613327049589 | Lipped Tibial Insert |
| 07613327049572 | Lipped Tibial Insert |
| 07613327049565 | Lipped Tibial Insert |
| 07613327049558 | Lipped Tibial Insert |
| 07613327049541 | Lipped Tibial Insert |
| 07613327049534 | Lipped Tibial Insert |
| 07613327049527 | Lipped Tibial Insert |
| 07613327049510 | Lipped Tibial Insert |
| 07613327049503 | Lipped Tibial Insert |
| 07613327049497 | Lipped Tibial Insert |
| 07613327049480 | Lipped Tibial Insert |
| 07613327049473 | Lipped Tibial Insert |
| 07613327049466 | Lipped Tibial Insert |
| 07613327049459 | Lipped Tibial Insert |
| 07613327049442 | Lipped Tibial Insert |
| 07613327049435 | Lipped Tibial Insert |
| 07613327049428 | Lipped Tibial Insert |
| 07613327049411 | Lipped Tibial Insert |
| 07613327049398 | Lipped Tibial Insert |
| 07613327049381 | Lipped Tibial Insert |
| 07613327048926 | Tibial Bearing Insert |
| 07613327048902 | Tibial Bearing Insert |
| 07613327048889 | Metal Backed Symmetric Patella |
| 07613327048872 | Distal Femoral Fixation Pegs |
| 07613327045086 | Titanium Fluted Stem |
| 07613327045079 | Titanium Fluted Stem |
| 07613327045062 | Titanium Fluted Stem |
| 07613327045055 | Titanium Fluted Stem |
| 07613327045048 | Titanium Fluted Stem |
| 07613327045031 | Titanium Fluted Stem |
Trademark Results [Duracon]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DURACON 97310997 not registered Live/Pending |
Careen, Inc. 2022-03-14 |
 DURACON 88711673 not registered Live/Pending |
POLYPLASTICS CO., LTD. 2019-12-02 |
 DURACON 86360015 not registered Dead/Abandoned |
POLYPLASTICS CO., LTD. 2014-08-07 |
 DURACON 86269768 not registered Dead/Abandoned |
J. H. Fenner & Co. Limited 2014-05-02 |
 DURACON 79013885 3136056 Live/Registered |
Vacuumschmelze GmbH & Co. KG 2005-02-10 |
 DURACON 78882100 3246984 Live/Registered |
Allied Mineral Products, Inc. 2006-05-12 |
 DURACON 78029023 2669126 Live/Registered |
Genest Concrete Works, Inc. 2000-10-04 |
 DURACON 76397289 2677868 Live/Registered |
Katun Corporation 2002-04-17 |
 DURACON 75935708 2756602 Live/Registered |
SURTREAT INNOVATIVE TECHNOLOGIES, LLC 2000-03-03 |
 DURACON 75564212 2351363 Live/Registered |
POLYPLASTICS CO., LTD. 1998-10-02 |
 DURACON 75401970 not registered Dead/Abandoned |
Scholle Corporation 1997-12-08 |
 DURACON 74483816 not registered Dead/Abandoned |
Ancor Marine Grade Electrical Products 1994-01-28 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.