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

CROSS LINKED POLYETHYLENE ACETABULAR COMPONENTS,MODEL XX-YY-ZZZZZZ

K Number: K990330 · Decision Mar 1, 2000
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
65
Review Days
393

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Basic Information

Device Name
CROSS LINKED POLYETHYLENE ACETABULAR COMPONENTS,MODEL XX-YY-ZZZZZZ
K Number
K990330
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implex Corp.
Date Received
February 2, 1999
Decision Date
March 1, 2000
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

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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. →