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

METAL BACKED ACETABULAR COMPONENT

K Number: K821342 · Decision May 21, 1982
Classifications
1
FEI Numbers
331
Registration Numbers
331
Same Product Code
83
Applicant Total
108
Review Days
16

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Basic Information

Device Name
METAL BACKED ACETABULAR COMPONENT
K Number
K821342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Intermedics Orthopedics
Date Received
May 5, 1982
Decision Date
May 21, 1982
Product Code
JOL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
JOL Catheter And Tip, Suction

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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 →