ClearanceBrief
Company ยท US

A.M. Surgical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2019. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EMFKnife, Surgical2
HRXArthroscope1
HTYPin, Fixation, Smooth1
HWCScrew, Fixation, Bone1
LXTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 16, 2019K191771SECURE Screw
A.M. Surgical, Inc.
HWC
Jul 17, 2019K191345Pegasus System
A.M. Surgical, Inc.
HRX
May 18, 2018K180087A.M. Surgical Intramedullary Fixation Device
A.M. Surgical, Inc.
HTY
Mar 13, 2008K080133MOUNTABLE ENDOSCOPIC BLADE
A.M. Surgical, Inc.
EMF
Oct 7, 2004K042458A.M. SURGICAL CPF DISTAL RADIAL EXTERNAL CROSS PIN FIXATION SYSTEM
A.M. Surgical, Inc.
LXT
Dec 30, 1998K982142MOUNTABLE ENDOSCOPIC KNIFE
A.M. Surgical, Inc.
EMF

Latest recalls

DateFirm and productCodeLinked 510(k)
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