ClearanceBrief
Company ยท US

Parallax Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2003. 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
MYUAccessory, Barium Sulfate, Methyl Methacrylate For Cranioplasty3
KNWInstrument, Biopsy2
GXPMethyl Methacrylate For Cranioplasty1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 12, 2003K033230TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TA
Parallax Medical, Inc.
MYU
Mar 11, 2003K023445TRACERS BONE CEMENT OPACIFIER
Parallax Medical, Inc.
MYU
Jul 25, 2002K022169CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES
Parallax Medical, Inc.
KNW
Jul 18, 2001K011206PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES
Parallax Medical, Inc.
KNW
Aug 31, 2000K994022PARALLAX CRANIOSET
Parallax Medical, Inc.
GXP
Aug 13, 1999K991893PARALLAX TRACER RADIOPAQUE PARTICLES
Parallax Medical, Inc.
MYU

Latest recalls

DateFirm and productCodeLinked 510(k)
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