Medrobotics Flex Robotic System— 510(k) K170453

Substantially Equivalent

Medrobotics Corporation

FDA 510(k) clearance K170453 for Medrobotics Flex Robotic System, Substantially Equivalent on 2017-10-19. Applicant: Medrobotics Corporation.

Clearance details

Applicant: Medrobotics Corporation
Product code: Code EOB
Advisory panel: Ear, Nose, Throat
Date received: 2017-02-15
Decision date: 2017-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EOB

product code EOB

Malfunction: 6,143
Total: 6,143

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.