FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODUILAR UNIPOLAR

K Number: K950998 · Decision Apr 13, 1995
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
22
Applicant Total
108
Review Days
41

Basic Information

Device Name
MODUILAR UNIPOLAR
K Number
K950998
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3400
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INTERMEDICS ORTHOPEDICS
Date Received
March 3, 1995
Decision Date
April 13, 1995
Product Code
KXA
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KXA Prosthesis, Hip, Femoral, Resurfacing

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Other Clearances by INTERMEDICS ORTHOPEDICS

K Number Device Name
K970300 NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI
K970498 NATURAL-KNEE II REVISION FEMORAL SPACER LUGS
K970166 NATURAL-HIP SYSTEM COCR REVISION STEM
K970567 SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS
K964357 NATURAL-HIP SYSTEM COCR STEM
K964350 MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA
K962190 PATELLOFEMORAL JOINT PROSTHESIS
K963266 NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED
K963155 INTERMOORE FRACTURE HIP STEM (MODIFY)
K962315 SELECT SHOULDER COCR HUMERAL STEM COMPONENT
Search all 108 clearances from INTERMEDICS ORTHOPEDICS →