Intermedics Orthopedics

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
108
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K970300NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTIJuly 3, 1997
K970498NATURAL-KNEE II REVISION FEMORAL SPACER LUGSApril 30, 1997
K970166NATURAL-HIP SYSTEM COCR REVISION STEMApril 8, 1997
K970567SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDSFebruary 27, 1997
K964357NATURAL-HIP SYSTEM COCR STEMJanuary 27, 1997
K964350MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMAJanuary 16, 1997
K962190PATELLOFEMORAL JOINT PROSTHESISOctober 28, 1996
K963266NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLAREDOctober 15, 1996
K963155INTERMOORE FRACTURE HIP STEM (MODIFY)October 1, 1996
K962315SELECT SHOULDER COCR HUMERAL STEM COMPONENTSeptember 3, 1996
K962289SELECT SHOULDER COCR HUMERAL STEM COMPONENTAugust 29, 1996
K962224SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTSAugust 28, 1996
K962101ZWEYMUELLER SL FEMORAL HIP STEMAugust 19, 1996
K962244SELECT SHOULDER PEGGED ALL-POLY GLENOIDAugust 9, 1996
K962238SELECT SHOULDER KEELED ALL-POLY GLENOIDSAugust 9, 1996
K960588WAGNER REVISION STEMAugust 5, 1996
K961921APR OVERSIZED HIP STEMAugust 5, 1996
K961727NATURAL-HIP SYSTEM - CALCAR REPLACEMENT HIP STEMJuly 19, 1996
K961799NATURAL HIP SYSTEM - DRG HIP STEMJuly 15, 1996
K960258NATURAL HIP SYSTEMJuly 12, 1996