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Orthopaedic Innovations, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020145ORTHOPAEDIC INNOVATIONS RENEWAL ACETABULAR CUP SYSTEMApril 15, 2002
K983881COBRA EXTERNAL FIXATORDecember 4, 1998
K962646PRIME MODULAR ENDO HEADSeptember 23, 1996
K960014PRACTIFIX EXTERNAL FIXATION SYSTEMMarch 18, 1996
K955620PRIME CEMENTED CALCAR FEMORAL STEMSFebruary 20, 1996
K955751PRIME FEMORAL CEMENT PLUGJanuary 26, 1996
K953033PRIME CEMENTED SMALL FEMORAL STEMSeptember 13, 1995
K940328PRIME CEMENTED HIP SYSTEMApril 7, 1995