
Chattanooga Group, Inc.
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TRITON is an FDA 510(k)-cleared medical device (K801643) manufactured by Chattanooga Group, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 27, 1980. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057