A.M. Surgical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
A.M. Surgical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 6 cleared submissions from 1998 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by A.M. Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by A.M. Surgical, Inc.
6 devices
Cleared
Oct 16, 2019
SECURE Screw
Orthopedic
106d
Cleared
Jul 17, 2019
Pegasus System
General & Plastic Surgery
58d
Cleared
May 18, 2018
A.M. Surgical Intramedullary Fixation Device
Orthopedic
126d
Cleared
Mar 13, 2008
MOUNTABLE ENDOSCOPIC BLADE
General & Plastic Surgery
55d
Cleared
Oct 07, 2004
A.M. SURGICAL CPF DISTAL RADIAL EXTERNAL CROSS PIN FIXATION SYSTEM
Orthopedic
27d
Cleared
Dec 30, 1998
MOUNTABLE ENDOSCOPIC KNIFE
General & Plastic Surgery
196d