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

101 UNIVERSAL ENDOPROSTHESIS

K Number: K823482 · Decision Feb 7, 1983
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
98
Applicant Total
108
Review Days
76

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Basic Information

Device Name
101 UNIVERSAL ENDOPROSTHESIS
K Number
K823482
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3390
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Intermedics Orthopedics
Date Received
November 23, 1982
Decision Date
February 7, 1983
Product Code
KWY
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
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Similar 510(k) Clearances

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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 →