| Primary Device ID | 00846795014439 | 
| NIH Device Record Key | a126ebda-4cc6-4c9a-9b75-c7df0e58a759 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Stablecut® Vanguard™ | 
| Version Model Number | 32700367 | 
| Company DUNS | 137354267 | 
| Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. | 
| 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 | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00846795014439 [Primary] | 
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2019-07-12 | 
| Device Publish Date | 2017-04-28 | 
| 00846795027408 | 32700389 | 
| 00846795027392 | 32700368 | 
| 00846795014446 | 32700369 | 
| 00846795014439 | 32700367 | 
| 00889024497405 | 32700389 | 
| 00889024497368 | 32700369 | 
| 00889024497351 | 32700368 | 
| 00889024497344 | 32700367 | 
| 00889024647640 | 32700369 | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() STABLECUT  85211274  3990180 Live/Registered  | 
        Synvasive Technology, Inc.  2011-01-05  | 
![]() STABLECUT  76393707  2672143 Dead/Cancelled  | 
        SYNVASIVE TECHNOLOGY, INC.  2002-04-09  | 
![]() STABLECUT  74299253  1758178 Dead/Cancelled  | 
        Sierra Surgical, Inc.  1992-07-28  |