| Primary Device ID | M6862100T11320 |
| NIH Device Record Key | ec768489-c401-4f22-bab2-6fe8e8193ae7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alamo P, Alamo T |
| Version Model Number | 2100T-1132 |
| Catalog Number | 2100T-1132 |
| Company DUNS | 962768169 |
| Company Name | ALLIANCE PARTNERS LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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(210)314-2525 |
| info@alliance-spine.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M6862100T11320 [Primary] |
| HTF | CURETTE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M6862100T11320]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-07 |
| Device Publish Date | 2017-01-01 |
| M6862100T11400 | Curette Instrument, Push Down |
| M6862100T11340 | Curette #4 Instrument, Straight |
| M6862100T11320 | Curette #2 Instrument, Straight |
| M6862100T11240 | Curette #4 Instrument, Right Angled |
| M6862100T11140 | Curette #4 Instrument, Left Angled |
| M6862100T11040 | Curette #4 Instrument, Reverse Angled |
| M6862100T11020 | Curette #2 Instrument, Reverse Angled |
| M6862100T10040 | Curette #4 Instrument, Forward Angled |
| M6862100T10020 | Curette #2 Instrument, Forward Angled |
| M6862100T13010 | Rasp Instrument, Angled |
| M6862100T13000 | Rasp Instrument, Straight |