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Lanx, LLC

FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K120399 LANX SPINAL FIXATION SYSTEMNKB2012-03-09 View
510(k) K102738 LANX FUSION SYSTEMOVD2011-02-10 View
510(k) K103040 LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)NKB2011-02-08 View
510(k) K093285 MODIFICATION TO LANX SPINAL FIXATION SYSTEMMNI2009-12-10 View
510(k) K082774 LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICEMAX2008-10-21 View
510(k) K073144 LANX INTERVERTEBRAL BODY FUSION DEVICEMAX2008-01-24 View
510(k) K071905 POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)KWQ2007-12-28 View
510(k) K071877 LANX SPINAL FIXATION SYSTEMMNI2007-09-17 View
510(k) K071633 LANX DEFORMITY SYSTEMKWP2007-08-15 View
510(k) K052384 LANX VBR SYSTEMMQP2005-10-07 View
510(k) K043484 LANX SPINAL FIXATION SYSTEMMNI2005-05-16 View
510(k) K050774 LANX ANTERIOR CERVICAL PLATE SYSTEMKWQ2005-04-11 View
510(k) K040401 LANX ANTERIOR CERVIAL PLATE SYSTEMKWQ2004-04-12 View
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