FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

101-32 FEMORAL COMPONENT

K Number: K813599 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
44
Applicant Total
108
Review Days
25

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Basic Information

Device Name
101-32 FEMORAL COMPONENT
K Number
K813599
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3320
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Intermedics Orthopedics
Date Received
December 28, 1981
Decision Date
January 22, 1982
Product Code
JDL
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
JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDL), 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 →