DIP Arthrodesis System— 510(k) K173616

Substantially Equivalent

In2bones Sas

FDA 510(k) clearance K173616 for DIP Arthrodesis System, Substantially Equivalent on 2018-01-19. Applicant: In2bones Sas.

Clearance details

Applicant: In2bones Sas
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 2017-11-22
Decision date: 2018-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ecully, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.