K243231 is an FDA 510(k) clearance for the Trigon PEEK HA Wedges. This device is classified as a Bone Wedge (Class II - Special Controls, product code PLF).
Submitted by Nvision Biomedical Technologies (San Antonio, US). The FDA issued a Cleared decision on November 8, 2024, 30 days after receiving the submission on October 9, 2024.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030. Intended To Be Used With Ancillary Fixation For Opening Wedge Osteotomies Or Fusion In The Ankle, Foot, Proximal Tibia..
| 510(k) Number | K243231 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 09, 2024 |
| Decision Date | November 08, 2024 |
| Days to Decision | 30 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | PLF - Bone Wedge |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |
| Definition | Intended To Be Used With Ancillary Fixation For Opening Wedge Osteotomies Or Fusion In The Ankle, Foot, Proximal Tibia. |