NEWMEDICAL MICRO BONE DISTRACTOR/FIXATOR— 510(k) K030485

Substantially Equivalent

Newmedical Technology, Inc.

FDA 510(k) clearance K030485 for NEWMEDICAL MICRO BONE DISTRACTOR/FIXATOR, Substantially Equivalent on 2003-12-03. Applicant: Newmedical Technology, Inc..

Clearance details

Applicant: Newmedical Technology, Inc.
Product code: Code MQN
Advisory panel: Dental
Date received: 2003-02-14
Decision date: 2003-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waukesha, WI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MQN

product code MQN

Injury: 346
Total: 346

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.