GNOMOS STEREOTACTIC DEVICE— 510(k) K901670

Substantially Equivalent

Medical Equipment Development Co., Inc.

FDA 510(k) clearance K901670 for GNOMOS STEREOTACTIC DEVICE, Substantially Equivalent on 1990-07-03. Applicant: Medical Equipment Development Co., Inc..

Clearance details

Applicant: Medical Equipment Development Co., Inc.
Product code: Code HAW
Advisory panel: Neurology
Date received: 1990-04-10
Decision date: 1990-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cinnaminson, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

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.