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

NATURAL POROUS HIP SYSTEM

K Number: K913060 · Decision Oct 11, 1991
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
108
Review Days
93

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Basic Information

Device Name
NATURAL POROUS HIP SYSTEM
K Number
K913060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intermedics Orthopedics
Date Received
July 10, 1991
Decision Date
October 11, 1991
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDI), ordered by most recent decision date.

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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 →