
Proact, Ltd.
Free shipping on orders over $99 · 30-day returns
BONE-TEMNO/STERNUM-TEMNO is an FDA 510(k)-cleared medical device (K913306) manufactured by Proact, Ltd.. This device is classified under the Unknown specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 31, 1991.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031