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

THE LPS - CONTINUUM TM HYBRID TIBIA, MODELS 32-5886-2Y-XX (ZIMMER) AND 05-119-XXYY1-0 (IMPLEX)

K Number: K012095 · Decision Jul 26, 2001
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
65
Review Days
21

Basic Information

Device Name
THE LPS - CONTINUUM TM HYBRID TIBIA, MODELS 32-5886-2Y-XX (ZIMMER) AND 05-119-XXYY1-0 (IMPLEX)
K Number
K012095
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IMPLEX CORP.
Date Received
July 5, 2001
Decision Date
July 26, 2001
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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

View all

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. →