| Primary Device ID | 07613327045383 | 
| NIH Device Record Key | 476cb828-6837-4e2d-ad7d-acec2165b7b5 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Exeter | 
| Version Model Number | 6309-2-240 | 
| Catalog Number | 6309-2-240 | 
| 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 | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Lumen/Inner Diameter | 22.2 Millimeter | 
| Outer Diameter | 40 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 07613327045383 [Primary] | 
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2015-09-24 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  EXETER  90559649  not registered Live/Pending | EQT AB 2021-03-04 | 
|  EXETER  87768494  not registered Live/Pending | Exeter Finance LLC 2018-01-24 | 
|  EXETER  87131287  not registered Dead/Abandoned | Reed, David 2016-08-08 | 
|  EXETER  86652227  5402003 Live/Registered | DataPoint International, LLC 2015-06-04 | 
|  EXETER  85911192  4610653 Live/Registered | DST Health Solutions, LLC 2013-04-22 | 
|  EXETER  85708626  4621652 Live/Registered | DST Health Solutions, LLC 2012-08-21 | 
|  EXETER  85612906  4877845 Dead/Cancelled | Exeter Finance Corp. 2012-05-01 | 
|  EXETER  81038864  1038864 Dead/Cancelled | Scott & Fetzer Company, The 0000-00-00 | 
|  EXETER  78070778  2765618 Live/Registered | XCaliber International Ltd., L.L.C. 2001-06-25 | 
|  EXETER  77779827  3728400 Live/Registered | Pyramex Safety Products, LLC 2009-07-13 | 
|  EXETER  77250908  3702155 Dead/Cancelled | BULOVA CORPORATION 2007-08-09 | 
|  EXETER  76654364  not registered Dead/Abandoned | Strathmore Partners LP 2006-01-27 |