Intermedics Orthopedics

FDA Regulatory Profile

Intermedics Orthopedics appears in FDA public data with 0 recalls, 108 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jul 3, 1997.

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/CSTIJul 3, 1997
K970498NATURAL-KNEE II REVISION FEMORAL SPACER LUGSApr 30, 1997
K970166NATURAL-HIP SYSTEM COCR REVISION STEMApr 8, 1997
K970567SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDSFeb 27, 1997
K964357NATURAL-HIP SYSTEM COCR STEMJan 27, 1997
K964350MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMAJan 16, 1997
K962190PATELLOFEMORAL JOINT PROSTHESISOct 28, 1996
K963266NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLAREDOct 15, 1996
K963155INTERMOORE FRACTURE HIP STEM (MODIFY)Oct 1, 1996
K962315SELECT SHOULDER COCR HUMERAL STEM COMPONENTSep 3, 1996
K962289SELECT SHOULDER COCR HUMERAL STEM COMPONENTAug 29, 1996
K962224SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTSAug 28, 1996
K962101ZWEYMUELLER SL FEMORAL HIP STEMAug 19, 1996
K962238SELECT SHOULDER KEELED ALL-POLY GLENOIDSAug 9, 1996
K962244SELECT SHOULDER PEGGED ALL-POLY GLENOIDAug 9, 1996
K960588WAGNER REVISION STEMAug 5, 1996
K961921APR OVERSIZED HIP STEMAug 5, 1996
K961727NATURAL-HIP SYSTEM - CALCAR REPLACEMENT HIP STEMJul 19, 1996
K961799NATURAL HIP SYSTEM - DRG HIP STEMJul 15, 1996
K960258NATURAL HIP SYSTEMJul 12, 1996