| Primary Device ID | 00195860016176 |
| NIH Device Record Key | 88f7e2fd-7612-40dd-8cc3-8b3a4f75f6d9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EMERGE Micro Anterior Cervical Plate System |
| Version Model Number | 101-1L12 |
| Catalog Number | 101-1L12 |
| Company DUNS | 116940934 |
| Company Name | Evolution Spine 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 | true |
| 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(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com | |
| Phone | +1(214)682-8536 |
| info@evolutionspine.com |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 12 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00195860016176 [Primary] |
| KWQ | Appliance, fixation, spinal intervertebral body |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
[00195860016176]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-06-21 |
| Device Publish Date | 2022-06-10 |
| 00195860016428 | DTS DRILL 20mm |
| 00195860016411 | DTS DRILL 18mm |
| 00195860016404 | DTS DRILL 16mm |
| 00195860016398 | DTS DRILL 14mm |
| 00195860016381 | DTS DRILL 12mm |
| 00195860016374 | DTS DRILL 10mm |
| 00195860016367 | INLINE INSERTER |
| 00195860016350 | INLINE INSERTER DRAWBAR |
| 00195860016268 | 2 LEVEL PLATE 30mm |
| 00195860016251 | 2 LEVEL PLATE 28mm |
| 00195860016244 | 2 LEVEL PLATE 26mm |
| 00195860016237 | 2 LEVEL PLATE 24mm |
| 00195860016220 | 2 LEVEL PLATE 22mm |
| 00195860016213 | 2 LEVEL PLATE 20mm |
| 00195860016206 | 2 LEVEL PLATE 18mm |
| 00195860016190 | 2 LEVEL PLATE 16mm |
| 00195860016183 | 2 LEVEL PLATE 14mm |
| 00195860016176 | 1 LEVEL PLATE 12mm |
| 00195860016169 | 1 LEVEL PLATE 11mm |
| 00195860016152 | 1 LEVEL PLATE 10mm |
| 00195860016145 | 1 LEVEL PLATE 9mm |
| 00195860016138 | 1 LEVEL PLATE 8mm |
| 00195860016121 | 1 LEVEL PLATE 7mm |
| 00195860016114 | 1 LEVEL PLATE 6mm |
| 00195860016107 | 1 LEVEL PLATE 5mm |
| 00195860016435 | DTS GUIDE 9mm |
| 00195860016343 | DTS GUIDE 12mm |
| 00195860016336 | DTS GUIDE 11mm |
| 00195860016329 | DTS GUIDE 10mm |
| 00195860016305 | DTS GUIDE 8mm |
| 00195860016299 | DTS GUIDE 7mm |
| 00195860016282 | DTS GUIDE 6mm |
| 00195860016275 | DTS GUIDE 5mm |