FDA.report

LEGION

Primary DI
00885556414705
Brand
LEGION
Company
Smith & Nephew, Inc.
Model
71423425
Catalog number
71423425
Device description
LEGION REVISION / HINGE HEMI STEPPED TIBIAL WEDGE SIZE 5-6 LEFT LATERAL/RIGHT MEDIAL 15MM
Published
2015-09-28
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

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

Premarket Submissions

SubmissionSupplement
K043440000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K043440000SMITH & NEPHEW, INC. REVISION KNEE SYSTEMSmith & Nephew, Inc.2005-02-18JWH

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00885556414705PrimaryGS10

GMDN Terms

TermDefinition
Knee arthroplasty wedgeA sterile device designed to augment the implantation of a knee femur or tibia prosthesis by acting as a space-filler adjacent to the prosthesis, typically to replace lost bone. It is typically made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo) or titanium (Ti)].

Sterilization Methods

Method

Contacts

PhoneEmail
+1(800)238-7538GUDID@SMITH-NEPHEW.COM

Regulatory Flags

DUNS number
109903521
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
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
false
Sterilization required before use
false

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00885556884140NA74038846740388462026-02-20

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Primary DIBrandCompanyProduct codePublished
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