FDA.report

GII

Primary DI
00885556808665
Brand
GII
Company
Smith & Nephew, Inc.
Model
E0017403-5
Catalog number
E0017403-5
Device description
GII FEMORAL REAM THROUGH CAM MODULE SZ 7
Published
2021-06-03
Public version status
New
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
HRYPROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

Product Code Classifications

CodeDeviceSpecialtyClass
HRYProsthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerOrthopedic2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00885556808665PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00885556808665008855568086658855568086650885556808665

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.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

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

Regulatory Flags

DUNS number
109903521
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

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00885556884140NA74038846740388462026-02-20

Other Devices Sharing Product Codes

Primary DIBrandCompanyProduct codePublished
00811767027779FREEDOM PARTIAL KNEEMAXX ORTHOPEDICS, INC.HRY2025-07-31
00811767027786FREEDOM PARTIAL KNEEMAXX ORTHOPEDICS, INC.HRY2025-07-31
00811767027793FREEDOM PARTIAL KNEEMAXX ORTHOPEDICS, INC.HRY2025-07-31
00811767027809FREEDOM PARTIAL KNEEMAXX ORTHOPEDICS, INC.HRY2025-07-31
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08033390281973PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
08033390281980PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
08033390281997PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
08033390282000PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
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08033390282055PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
08033390282062PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
08033390282079PHYSICA POROUS CR - CoCrMo + PoroTiLIMACORPORATE SPAHRY2025-07-09
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