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

CABLE-EASE PLATE AND CABLE SYSTEM - TROCHANTERIC HOOK

K Number: K950027 · Decision Mar 6, 1995
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
108
Review Days
61

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Basic Information

Device Name
CABLE-EASE PLATE AND CABLE SYSTEM - TROCHANTERIC HOOK
K Number
K950027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Intermedics Orthopedics
Date Received
January 4, 1995
Decision Date
March 6, 1995
Product Code
JDQ
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
JDQ Cerclage, Fixation

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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 →