UDI device identifier
TRESTLE LUXE 722-24522
UDI device identifier 00190376217079 · ALPHATEC SPINE, INC.
Key facts
| Primary DI | 00190376217079 |
|---|---|
| Brand name | TRESTLE LUXE |
| Version or model | 722-24522 |
| Company | ALPHATEC SPINE, INC. |
| DUNS number | 602465783 |
| Product code | KWQ |
| GMDN term | Spinal fixation plate, non-bioabsorbable |
| Premarket submission | K102820 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | Yes |
| Publish date | Nov 6, 2019 |
| Version date | Nov 20, 2025 |
| Description | 4.5MM VARIABLE ANGLE, SELF-DRILLING SCREW, 22 MM |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: