FDA.report

MAXIM KNEE SYSTEM

Primary DI
05019279465675
Brand
MAXIM KNEE SYSTEM
Company
Biomet Uk Ltd
Model
32-345381
Catalog number
32-345381
Published
2017-07-28
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
HWTTEMPLATE

Product Code Classifications

CodeDeviceSpecialtyClass
HWTTemplateOrthopedic1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
05019279465675PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
05019279465675050192794656755019279465675

GMDN Terms

TermDefinition
Knee femur prosthesis trialA copy of a final femur prosthesis designed to be used during unicompartmental knee replacement surgery or total knee arthroplasty (TKA) to determine the correct alignment, size, and fit of the final prosthesis. It is one of a set, or a set, of graduated sizes, and may be used in conjunction with a knee tibia trial prosthesis and a patella trial prosthesis. It is typically made of metal or polymer material and includes femoral articulation trials, femoral spacer trials, femoral wedge/augment trials, anterior stop trials, stem adaptor trials, and stem trials. This is a reusable device intended to be sterilized prior to use.

Device Sizes

TypeValueUnit
Device Size Text, specify0

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(800)348-9500customerservice@zimmerbiomet.c
+1(800)348-9500customerservice@zimmerbiomet.com

Regulatory Flags

DUNS number
219322575
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company

Primary DIBrandModelCatalogPublished
05019279477333Oxford Partial Knee SystemFemoral Impactor32-42012732-4201272020-05-23
05019279905638OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL IMPACTOR32-42093232-4209322020-05-23
05019279439935Oxford® Partial Knee System32-42297432-4229742020-05-23
05019279439942Oxford® Partial Knee System32-42297532-4229752020-05-23
05019279439959Oxford® Partial Knee System32-42297632-4229762020-05-23
00880304525672Oxford® Partial Knee System32-42209732-4220972025-01-10
00887868259050Oxford® Partial Knee System1100317791100317792025-01-10
00887868354694Oxford® Partial Knee System1665701665702025-01-10
00887868354700Oxford® Partial Knee System1665711665712025-01-10
00887868354717Oxford® Partial Knee System1665721665722025-01-10
00887868354724Oxford® Partial Knee System1665731665732025-01-10
00887868354731Oxford® Partial Knee System1665741665742025-01-10
00887868354748Oxford® Partial Knee System1665751665752025-01-10
00887868354755Oxford® Partial Knee System1665761665762025-01-10
00887868354762Oxford® Partial Knee System1665771665772025-01-10
00887868354779Oxford® Partial Knee System1665781665782025-01-10
00887868354786Oxford® Partial Knee System1665791665792025-01-10
00887868354793Oxford® Partial Knee System1665801665802025-01-10
00887868354809Oxford® Partial Knee System1665811665812025-01-10
00887868354816Oxford® Partial Knee System1668451668452025-01-10

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