Footmotion HammerToe— 510(k) K172485

Substantially Equivalent

Newclip Technics

FDA 510(k) clearance K172485 for Footmotion HammerToe, Substantially Equivalent on 2018-03-02. Applicant: Newclip Technics.

Clearance details

Applicant: Newclip Technics
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 2017-08-17
Decision date: 2018-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haute-Goulaine, 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.