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Ebi, L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
95
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K100438POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEMJune 23, 2010
K100220POLARIS SPINAL SYSTEMMay 17, 2010
K093880PEANUT GROWTH CONTROL PLATING SYSTEMApril 16, 2010
K092574ESL SPINAL SYSTEMFebruary 4, 2010
K093057BIOMET VISION FOOTRING SYSTEMDecember 1, 2009
K092336C-THRU SPINAL SYSTEMOctober 15, 2009
K091381IBEX SPINAL SYSTEMAugust 7, 2009
K0902035.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTSJuly 30, 2009
K090523POLARIS SPINAL SYSTEMJuly 1, 2009
K082406EXPANDABLE PEEK-OPTIMA IMPLANTJanuary 14, 2009
K082187BIOMET ANTERIOR LUMBAR PLATENovember 13, 2008
K063346PRO OSTEON 500RApril 18, 2007
K062494EBI OPTILOCK UPPER EXTREMITY PLATING SYSTEMOctober 19, 2006
K062810SOLITAIRE ANTERIOR SPINAL SYSTEMOctober 17, 2006
K062685EBI ARAY SPINAL SYSTEMOctober 6, 2006
K061978EBI, L.P.'S LINE EXTENSION TO THE ARRAY SPINAL SYSTEMAugust 11, 2006
K061441EBI 5.5 HELICAL FLANGE SPINAL SYSTEMJuly 25, 2006
K061563EBI ARRAY SPINAL SYSTEMJune 23, 2006
K061016EBI ESL PEEK-OPTIMA SPINE SYSTEMJune 8, 2006
K061098EBI OPTILOCK PERIARTICULAR PLATING SYSTEMMay 24, 2006