Stage— 510(k) K223079

Substantially Equivalent

Spintech, Inc.

FDA 510(k) clearance K223079 for Stage, Substantially Equivalent on 2022-10-28. Applicant: Spintech, Inc..

Clearance details

Applicant: Spintech, Inc.
Product code: Code LNH
Advisory panel: Radiology
Date received: 2022-09-30
Decision date: 2022-10-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Bingham Farms, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

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.