LOT: 2120037403.

Shelf shed 3 box 21 #2.

Biomet CP500141 Diamond Point Femur Awl Orthopedic The sale of this item may be subject by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item. Any used product has been cleaned/sterilized per manufacturers specifications.

00-2490-008-01 Small Antegrade Femoral Connecting Bolt 2. 00-2490-098-10 Small Antegrade Femur Targeting Guide. 00-2490-091-15 Small Antegrade Femur Interlock Module. 00-2490-091-16 Small Antegrade Femur Recon Screw Module.

Zimmer Biomet – Osteotome REF:2821-02 – 3/8 In (9mm) Used. Distal ends remain in good shape. Average sharpness on the tip. A lot of cosmetic wear and tear but overall in good condition.

ZIMMER BIOMET 32-485501 Vangaurd TIB Template Assembly Brand new in sealed package ANY QUESTIONS, PLEASE DON’T HESITATE CONTACTING USFAST, SAME DAY SHIPPING FOLLOWING PAYMENT M “The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.”

The Zimmer Biomet ZDRIVE High Torque Driver 70-2001 is a premium surgical and orthopedic instrument designed for precision and efficiency in medical procedures. Manufactured by Zimmer, a trusted brand in the healthcare industry, this high torque driver offers reliable performance and durability. With its model number 70-2001, this instrument is specifically designed for use in various surgical and orthopedic applications, providing healthcare professionals with a reliable tool for achieving desired outcomes in patient care. Driver with battery. Nearly new condition.

“The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. exporter only . Once it is signed for by the U.S. Exporter we are no longer responsible for the item.

Reprocessing will be required before patient use. No exceptions.

I don’t know much about this, so please look at all the pictures and let me know if you need to see more pictures. Thank you!!