MuscleView 2.0

MuscleView 2.0 is an FDA 510(k)-cleared medical device (K251682) manufactured by Springbok, Inc. (Dba Springbok Analytics). This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 8, 2025. Regulation: 8.