EXETER 0580-3-501
GUDID 07613327123845
EXETER STEM V40
Howmedica Osteonics Corp.
Uncoated hip femur prosthesis, modular| Primary Device ID | 07613327123845 |
| NIH Device Record Key | d9e6e878-899e-40e1-be64-40e9eba05f28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXETER |
| Version Model Number | 0580-3-501 |
| Catalog Number | 0580-3-501 |
| 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 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 125 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327123845 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K173499
FDA Product Code
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-05-03 |
On-Brand Devices [EXETER]
Trademark Results [EXETER]
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 |
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