| Primary Device ID | 00841379186168 |
| NIH Device Record Key | 85c7e16c-b42c-4278-b91c-28621ab2cf21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | GZB10SZ10 |
| Catalog Number | GZB10SZ10 |
| Company DUNS | 073029645 |
| Company Name | HYHTE HOLDINGS, INC. |
| 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 | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com | |
| Phone | 760-814-8047 |
| troy@asturamedical.com |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Length | 10 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841379186168 [Primary] |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
[00841379186168]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-07-21 |
| Device Publish Date | 2021-07-13 |
| 00841379164388 | TLIF SPACER |
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| 00841379139898 | OTLIF SPACER, PEEK, 10MMX22MMX08MMX5°, NON-STERILE |
| 00841379100614 | OTLIF SPACER, PEEK, 10MMX22MMX14MMX5°, NON-STERILE |
| 00841379100607 | OTLIF SPACER, PEEK, 10MMX22MMX13MMX5°, NON-STERILE |
| 00841379100584 | OTLIF SPACER, PEEK, 10MMX22MMX11MMX5°, NON-STERILE |
| 00841379100577 | OTLIF SPACER, PEEK, 10MMX22MMX10MMX5°, NON-STERILE |
| 00841379100560 | OTLIF SPACER, PEEK, 10MMX22MMX09MMX5°, NON-STERILE |
| 00841379100553 | OTLIF SPACER, PEEK, 10MMX22MMX07MMX5°, NON-STERILE |
| 00841379100546 | TLIF SPACER |
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