Signus Medizintechnik GmbH
TETRIS II
SKU K122317UPC MAX
In Stock
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IIFDA 510(k) Cleared (K122317)
1
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Signus Medizintechnik GmbH
Free shipping on orders over $99 · 30-day returns
TETRIS II is an FDA 510(k)-cleared medical device (K122317) manufactured by Signus Medizintechnik GmbH. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 28, 2012. Regulation: 8.
