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

TRABECULAR METAL KNEE SYSTEM AUGMENTS

K Number: K040487 · Decision Dec 21, 2004
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
65
Review Days
300

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Basic Information

Device Name
TRABECULAR METAL KNEE SYSTEM AUGMENTS
K Number
K040487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implex Corp.
Date Received
February 25, 2004
Decision Date
December 21, 2004
Product Code
MBH
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
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MBH), ordered by most recent decision date.

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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
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
K032282 MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM
Search all 65 clearances from Implex Corp. →