| Primary Device ID | 00887517727923 |
| NIH Device Record Key | 406cea2b-2551-437a-80d1-90f2a0a466e0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Halo Buttress Plate |
| Version Model Number | 7890032 |
| Company DUNS | 053950783 |
| Company Name | Nuvasive, 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 | 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(858)909-1800 |
| RA_UDI@nuvasive.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517727923 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517727923]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-25 |
| Device Publish Date | 2019-12-17 |
| 00887517727930 | ALIF Buttress Plate Awl |
| 00887517727923 | ALIF Buttress Plate Inserter |
| 00887517789969 | ALIF Buttress Plate Tray |
| 00887517728029 | ALIF Buttress Plate, 27mm |
| 00887517728012 | ALIF Buttress Plate, 25mm |
| 00887517728005 | ALIF Buttress Plate, 23mm |
| 00887517727992 | ALIF Buttress Plate, 21mm |
| 00887517727985 | ALIF Buttress Plate Driver, Final |
| 00887517727978 | ALIF Buttress Plate Screwdriver |
| 00887517727961 | ALIF Buttress Plate Tap, 5.75mm |
| 00887517727954 | ALIF Buttress Plate Tap, 4.75mm |
| 00887517727947 | ALIF Buttress Plate Bender |