SKELETAL FIXATION PIN— 510(k) K895173

Name: FDA 510(k) clearance K895173
Creator: U.S. Food and Drug Administration
Published: 1989-09-12

Substantially Equivalent

Kronner Medical

FDA 510(k) clearance K895173 for SKELETAL FIXATION PIN, Substantially Equivalent on 1989-09-12. Applicant: Kronner Medical. Device class: 2.

Clearance details

Applicant: Kronner Medical
Product code: Code JDW
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1989-08-10
Decision date: 1989-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roseburg, OR, US

Download summary PDF View on FDA.gov ↗

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More clearances from Kronner Medical

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K894228 — KRONNER SPHERICAL CUTTERS1990-07-23
K895171 — BLOOD GAS SAFETY SYRINGE1989-11-07
K895172 — KRONNER SACRAL PIN GUIDE1989-09-12
K871248 — KRONNER COLLES-FOREARM EXTERNAL FIXATION1987-06-03
K871247 — KRONNER UNIVERSAL FRAME EXTERNAL FIXATION1987-05-22

Adverse events under product code JDW

product code JDW

Injury: 717
Total: 717

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.