Buckman Co., Inc.
Buckman Co., Inc. — FDA 510(k) Submissions
Buckman Co., Inc. has submitted 111 FDA 510(k) premarket notifications since 1983, of which 104 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Screw, Fixation, Bone, Exerciser, Powered, Powered Laser Surgical Instrument, Appliance, Fixation, Spinal Interlaminal, Pin, Fixation, Threaded . Use the specialty filter in the sidebar to narrow results.
Looking for a specific device from Buckman Co., Inc.? Search by device name or K-number.
Search all Buckman Co., Inc. devices