| Primary Device ID | 07613252633259 | 
| NIH Device Record Key | d7ad4b0c-5d22-412f-a590-9b3cc0c671d6 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | CinchLock | 
| Version Model Number | CAT02514 | 
| Catalog Number | CAT02514 | 
| Company DUNS | 187502109 | 
| Company Name | STRYKER CORPORATION | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| MRI Safety Status | Labeling does not contain MRI Safety Information | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| 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 | 
| Phone | +1(866)624-4422 | 
| xx@xx.xx | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 07613252633259 [Primary] | 
| HTW | BIT, DRILL | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[07613252633259]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-11-22 | 
| Device Publish Date | 2015-09-09 | 
| 07613252633259 | CINCHLOCK SS REUSABLE DRILL BIT | 
| 07613252633235 | CINCHLOCK SS DRILL BIT | 
| 07613252633228 | FG, CINCHLOCK SS ANCHOR WITH INSERTER | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  CINCHLOCK  85773291  4416009 Live/Registered | STRYKER PUERTO RICO LIMITED 2012-11-07 | 
|  CINCHLOCK  74661398  2011219 Dead/Cancelled | Rovac Corporation, The 1995-04-14 |