
Biomet Microfixation
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2.1 x 255mm Drill, 22mm Stop is an FDA 510(k)-cleared medical device (K223199) manufactured by Biomet Microfixation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 14, 2022. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280