EVOLVE MODULAR RADIAL HEAD— 510(k) K060731
Substantially EquivalentWrightmedicaltechnologyinc
FDA 510(k) clearance K060731 for EVOLVE MODULAR RADIAL HEAD, Substantially Equivalent on 2006-04-19. Applicant: Wrightmedicaltechnologyinc. Device class: 2.
Clearance details
- Applicant
- Wrightmedicaltechnologyinc
- Product code
- Code KWI
- Device class
- Class 2
- Regulation
- 21 CFR 888.3170
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Arlington, TN, US
Recent devices under product code KWI
view allMore clearances from Wrightmedicaltechnologyinc
view allAdverse events under product code KWI
product code KWI- Injury
- 490
- Total
- 490
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K060731
K-number listed on FDA's recall record- Z-0005-2023 — stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
- Z-0006-2023 — stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
- Z-2989-2020 — EVOLVE STEM 8.5MM Model # 496S085
- Z-1101-2020 — WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220
- Z-1102-2020 — WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K060731.
Data sourced from openFDA. This site is unofficial and independent of the FDA.