UDI device identifier
A-CIFT® SoloFuse® 01-32020-07-HA
UDI device identifier 00190361023678 · SPINEFRONTIER, INC.
Key facts
| Primary DI | 00190361023678 |
|---|---|
| Brand name | A-CIFT® SoloFuse® |
| Version or model | 01-32020-07-HA |
| Company | SPINEFRONTIER, INC. |
| DUNS number | 002003243 |
| Product code | OVE |
| GMDN term | Polymeric spinal interbody fusion cage |
| Premarket submission | K172484 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Aug 31, 2018 |
| Version date | Feb 24, 2020 |
| Description | A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm Wide, 7mm Height HA PEEK |
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: