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

CONSENSUS KNEE SYSTEM

K Number: K102927 · Decision Jan 26, 2011
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
17
Review Days
114

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Basic Information

Device Name
CONSENSUS KNEE SYSTEM
K Number
K102927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Consensus Orthopedics, Inc.
Date Received
October 4, 2010
Decision Date
January 26, 2011
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 Consensus Orthopedics, Inc.

K Number Device Name
K170344 Tahoe Uni Knee System
K163167 CKS Plus Knee System
K160515 PS2 Knee System
K143725 Consensus Knee System Modular Tibial Baseplate
K133919 CONSENSUS VITALITE TIBIAL INSERT
K141043 CS2 MULTI-HOLE ACETABULAR SHELL
K130652 VITALITE E CROSS-LINKED POLYETHYLENE ACETABULAR INSERT
K122512 CS2 HIP SYSTEM
K120595 UNISYN PLUS HIP STEM
K121935 TAPERSET HIP SMALL STEMS
Search all 17 clearances from Consensus Orthopedics, Inc. →