| Primary Device ID | 07613327050165 | 
| NIH Device Record Key | 68c21189-e80d-4a57-9fbd-90c0d7d1bec4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Wichita | 
| Version Model Number | 6647-3-150 | 
| Catalog Number | 6647-3-150 | 
| 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 Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 50 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 07613327050165 [Primary] | 
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES | 
| 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 | 
| 07613327050189 | Self Tapping Screw | 
| 07613327050172 | Self Tapping Screw | 
| 07613327050165 | Self Tapping Screw | 
| 07613327050158 | Self Tapping Screw | 
| 07613327050141 | Self Tapping Screw | 
| 07613327050134 | Self Tapping Screw | 
| 07613327050127 | Self Tapping Screw | 
| 07613327050110 | Self Tapping Screw | 
| 07613327050103 | Compression Screw | 
| 07613327045116 | Fusion Nail | 
| 07613327045093 | Femoral Component | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  WICHITA  77296882  not registered Dead/Abandoned | Greater Wichita Convention and Tourism Bureau, Inc. 2007-10-05 | 
|  WICHITA  75239663  2166585 Live/Registered | HOWMEDICA OSTEONICS CORP. 1997-02-10 | 
|  WICHITA  74712457  1991254 Dead/Cancelled | Andersen Corporation 1995-08-08 | 
|  WICHITA  74202402  not registered Dead/Abandoned | PLAYBOY ENTERPRISES, INC. 1991-09-11 | 
|  WICHITA  73753251  1565483 Live/Registered | DANA CORPORATION 1988-08-29 | 
|  WICHITA  73687911  1524167 Dead/Cancelled | W-W GRINDER, INC. 1987-10-05 | 
|  WICHITA  73248558  1197061 Dead/Cancelled | Wichita Engineering & Supply, Inc. 1980-02-04 | 
|  WICHITA  73214361  1153662 Dead/Cancelled | Dana Corporation 1979-05-04 |