
Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
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CODA Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K230993) manufactured by Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 19, 2023. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057