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Trinity Orthopedics, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K081790 MODIFICATION TO SINGLE PLANAR MULTI AXIS (SPMA) PEDICLE SCREW SYSTEMMNI2008-07-24 View
510(k) K070295 SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEMMNI2007-05-21 View
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