Interphalangeal Joint Fusion Device Range— 510(k) K191424

Substantially Equivalent

Neosteo

FDA 510(k) clearance K191424 for Interphalangeal Joint Fusion Device Range, Substantially Equivalent on 2019-08-28. Applicant: Neosteo.

Clearance details

Applicant: Neosteo
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 2019-05-29
Decision date: 2019-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nantes, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.