ClearanceBrief
Company ยท US

Immedica, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2003. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
LXTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite6
GXPMethyl Methacrylate For Cranioplasty1
JDWPin, Fixation, Threaded1
LODBone Cement1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 22, 2003K023575CONCERT CRANIOPLAST
Immedica, Inc.
GXP
Feb 8, 2002K013755CONCERT RADIOPAQUE BONE CEMENT
Immedica, Inc.
LOD
Dec 15, 2000K003205TRANSFX ANGLED RODS
Immedica, Inc.
LXT
Jul 7, 2000K001228EXTERNAL FIXATION ANCHOR PIN
Immedica, Inc.
JDW
Jun 15, 2000K001084TRANS FX ADJUSTABLE PIN TO BAR CLAMP
Immedica, Inc.
LXT
Jul 22, 1999K991723TRANSFX MULTI PIN CLAMP
Immedica, Inc.
LXT
May 17, 1999K990848TRANSFX INTERMEDIATE EXTERNAL FIXATION SYSTEM,TRANSFX SMALL EXTERNAL FIXATION SYSTEM, TRANSFX MINI EXTERNAL FIXATION
Immedica, Inc.
LXT
Mar 4, 1999K984357TRANSFX EXTERNAL FIXATION SYSTEM
Immedica, Inc.
LXT

Latest recalls

DateFirm and productCodeLinked 510(k)
Jun 5, 2003Immedica Inc
TransFx Pin, External Fixation Pin. 3.0 /4.0 mm x 80mm, 20mm thread.
Terminated
LXTK990848
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