| Primary Device ID | 00880304481978 |
| NIH Device Record Key | 086660a5-eee3-4aa4-a243-cab28291d707 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VANGUARD SSK360/DA360 KNEE SYSTEM |
| Version Model Number | 185268 |
| Catalog Number | 185268 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304481978 [Primary] |
| MBV | Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2015-10-24 |
| 00880304482128 | 185287 |
| 00880304482111 | 185285 |
| 00880304482104 | 185283 |
| 00880304482098 | 185281 |
| 00880304482081 | 185290 |
| 00880304482074 | 185288 |
| 00880304482067 | 185286 |
| 00880304482050 | 185284 |
| 00880304482043 | 185282 |
| 00880304482036 | 185280 |
| 00880304482029 | 185267 |
| 00880304482012 | 185265 |
| 00880304482005 | 185263 |
| 00880304481992 | 185261 |
| 00880304481985 | 185270 |
| 00880304481978 | 185268 |
| 00880304481961 | 185266 |
| 00880304481954 | 185264 |
| 00880304481947 | 185262 |
| 00880304467422 | 185260 |