ClearanceBrief
Company ยท US

Johnson & Johnson

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2012. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MAXIntervertebral Fusion Device With Bone Graft, Lumbar4
NKBThoracolumbosacral Pedicle Screw System3
GZTRetractor, Self-Retaining, For Neurosurgery2
HWCScrew, Fixation, Bone1
MBIFastener, Fixation, Nondegradable, Soft Tissue1
MEDSterilant, Medical Devices1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 27, 2012K113273SPOTLIGHT ACCESS SYSTEM
Johnson & Johnson
GZT
Dec 16, 2011K112913SPOTLIGHT ACCESS SYSTEM
Johnson & Johnson
GZT
Dec 13, 2011K113348COUGAR SYSTEM
Johnson & Johnson
MAX
Oct 26, 2011K110551EXPEDIUM SPINE SYSTEM
Johnson & Johnson
NKB
Oct 11, 2011K110694CONCORDE BULLET SPINAL SYSTEM
Johnson & Johnson
MAX
Jul 6, 2011K111571VIPER SYSTEMS
Johnson & Johnson
NKB
May 13, 2011K110454COUGAR LS LATERAL CAGE SYSTEM
Johnson & Johnson
MAX
Mar 17, 2011K103743CONCORDE CURVE SYSTEM
Johnson & Johnson
MAX
Feb 17, 2011K103490EXPEDIUM SPINE SYSTEM, MOSS MIAMI SPINE SYSTEM
Johnson & Johnson
NKB
Jan 25, 2007K063577FEMORAL INTRAFIX SCREW AND SHEATH
Johnson & Johnson Company
MBI
Jun 9, 2006K060914TRIDENT ANCHOR
Johnson & Johnson Company
HWC
Apr 12, 2006K060618CIDEX ACTIVATED DIALDEHYDE SOLUTION
Johnson & Johnson Co.
MED

Latest recalls

DateFirm and productCodeLinked 510(k)
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