FDA.report

Revision Knee System

Primary DI
00844588014147
Brand
Revision Knee System
Company
CONSENSUS ORTHOPEDICS, INC.
Model
2432-0-0006
Catalog number
2432-0-0006
Device description
Tibial Baseplate, Cemented
Published
2015-10-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Contact Domains

Product Codes

CodeName
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Product Code Classifications

CodeDeviceSpecialtyClass
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerOrthopedic2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00844588014147PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00844588014147008445880141478445880141470844588014147

GMDN Terms

TermDefinition
Uncoated knee tibia prosthesis, metallicAn implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with an insert and/or the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement.

Device Sizes

TypeValueUnit
Device Size Text, specify0

Sterilization Methods

Method

Contacts

PhoneEmail
+1(916)355-7100zjohnson@consensusortho.com

Regulatory Flags

DUNS number
824905723
Device count
1
DM exempt
true
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
true
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company

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00844588044311TracPatch4000-0-10004000-0-10002020-03-26
00844588006111Consensus® Knee System2151-0-00012151-0-00012015-10-05
00844588006128Consensus® Knee System2151-0-00022151-0-00022015-10-05
00844588006135Consensus® Knee System2151-0-00032151-0-00032015-10-05
00844588006142Consensus® Knee System2151-0-00042151-0-00042015-10-05
00844588006159Consensus® Knee System2151-0-00052151-0-00052015-10-05
00844588006166Consensus® Knee System2151-0-00062151-0-00062015-10-05
00844588006173Consensus® Knee System2152-0-00012152-0-00012015-10-05
00844588006180Consensus® Knee System2152-0-00022152-0-00022015-10-05
00844588006197Consensus® Knee System2152-0-00032152-0-00032015-10-05
00844588006203Consensus® Knee System2152-0-00042152-0-00042015-10-05
00844588006210Consensus® Knee System2152-0-00052152-0-00052015-10-05
00844588006227Consensus® Knee System2152-0-00062152-0-00062015-10-05
00844588006234Consensus® Knee System2153-0-00012153-0-00012015-10-05
00844588006241Consensus® Knee System2153-0-00022153-0-00022015-10-05
00844588006258Consensus® Knee System2153-0-00032153-0-00032015-10-05
00844588006265Consensus® Knee System2153-0-00042153-0-00042015-10-05
00844588006272Consensus® Knee System2153-0-00052153-0-00052015-10-05
00844588006289Consensus® Knee System2153-0-00062153-0-00062015-10-05
00844588006296Consensus® Knee System2154-0-00012154-0-00012015-10-05

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