| Primary Device ID | 00810086191154 |
| NIH Device Record Key | 574f9ec1-84fa-444a-9562-8a42791937ab |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PLS |
| Version Model Number | PLS-530T57 |
| Company DUNS | 079917057 |
| Company Name | SINTEA USA, 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 | false |
| OTC Over-The-Counter | false |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com | |
| Phone | 3054906850 |
| info@sinteausa.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810086191154 [Primary] |
| KWP | Appliance, Fixation, Spinal Interlaminal |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
[00810086191154]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-12 |
| Device Publish Date | 2024-12-04 |
| 00810086190867 | DUAL LEAD SCREW DIAMETER 5 MM - LENGTH 35 MM |
| 00810086193714 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.55mm-ø8mm |
| 00810086193691 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.45mm-ø8mm |
| 00810086193554 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.50mm-ø7mm |
| 00810086193547 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.45mm-ø7mm |
| 00810086193400 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.50mm-ø6mm |
| 00810086193394 | 3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.45mm-ø6mm |
| 00810086191161 | Dual Lead Screw Ø7 L35mm |
| 00810086191154 | Dual Lead Screw Ø7 L30mm |
| 00810086191055 | Dual Lead Screw Ø6 L55mm |
| 00810086191000 | Dual Lead Screw Ø6 L30mm |
| 00810086190898 | Dual Lead Screw Ø5 L50mm |
| 00810086190881 | Dual Lead Screw Ø5 L45mm |
| 00810086190874 | Dual Lead Screw Ø5 L40mm |
| 00810086190737 | Dual Lead Screw ø4mm L45mm |
| 00810086190713 | Dual Lead Screw ø4mm L35mm |
| 00810086190706 | Dual Lead Screw ø4mm L30mm |
| 00810086190720 | Dual Lead Screw ø4mm L40mm |