| Primary Device ID | 00846795027392 |
| NIH Device Record Key | 49b284b3-1c30-4325-8e68-69e29e6b2506 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Stablecut® Vanguard™ |
| Version Model Number | 32700368 |
| 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 | 00846795027392 [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 |