MuscleView— 510(k) K241331

Substantially Equivalent

Springbok, Inc.

FDA 510(k) clearance K241331 for MuscleView, Substantially Equivalent on 2024-10-01. Applicant: Springbok, Inc..

Clearance details

Applicant: Springbok, Inc.
Product code: Code LNH
Advisory panel: Radiology
Date received: 2024-05-10
Decision date: 2024-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Charlottesville, VA, 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.