WishBone K-Wire System— 510(k) K173013

Substantially Equivalent

Wishbone Medical, Inc.

FDA 510(k) clearance K173013 for WishBone K-Wire System, Substantially Equivalent on 2017-12-14. Applicant: Wishbone Medical, Inc..

Clearance details

Applicant: Wishbone Medical, Inc.
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 2017-09-27
Decision date: 2017-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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.