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

IMPLEX BIPOLAR HIP SYSTEM

K Number: K970447 · Decision Apr 30, 1997
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
98
Applicant Total
65
Review Days
83

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Basic Information

Device Name
IMPLEX BIPOLAR HIP SYSTEM
K Number
K970447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3390
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Implex Corp.
Date Received
February 6, 1997
Decision Date
April 30, 1997
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

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Other Clearances by Implex Corp.

K Number Device Name
K051978 TRABECULAR METAL VERTEBRAL BODY REPLACEMENT
K051196 TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1
K040487 TRABECULAR METAL KNEE SYSTEM AUGMENTS
K040630 TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ
K040756 THE TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 10-340-XXXXX
K031962 NEXGEN TRABECULAR METAL TIBIAL CONE AUGMENTS
K033384 THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 06-165-ZZZZ
K032527 HEDROCEL VERTEBRAL BODY REPLACEMENT
K032344 THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330
K031449 MODIFICATION TO THE TRABECULAR METAL GLENOID - BIGLIANI/FLATOW THE COMPLETE SHOULDER SOLUTION
Search all 65 clearances from Implex Corp. →