FDA.reportPublic FDA data

FREEDOM KNEE CEMENTLESS

Primary DI
00811767024983
Brand
FREEDOM KNEE CEMENTLESS
Company
MAXX ORTHOPEDICS, INC.
Model
PFCRLH00-PK
Device description
Cementless Femoral Size H, CR, Left
Published
2015-10-13
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K150680000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K150680000Freedom Cementless Femoral ComponentMaxx Orthopedics, Inc.2015-06-26MBH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00811767024983PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00811767024983008117670249838117670249830811767024983

GMDN Terms#

Term, Definition table
TermDefinition
Coated knee femur prosthesisA sterile implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr)] and is coated with a material (e.g., beads, hydroxyapatite, mesh) intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation may be performed with or without bone cement.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Depth80Millimeter
Length74Millimeter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
792030103
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810008128749LibertasMO-SFCC-28/062025-07-31
00810008128756LibertasMO-SFCC-28/072025-07-31
00810008128763LibertasMO-SFCC-28/082025-07-31
00810008128770LibertasMO-SFCC-28/092025-07-31
00810008128787LibertasMO-SFCC-28/102025-07-31
00810008128794LibertasMO-SFCC-28/112025-07-31
00810008128800LibertasMO-SFCC-28/122025-07-31
00810008128817LibertasMO-SFCC-28/132025-07-31
00810008128824LibertasMO-SFCC-28/142025-07-31
00810008128831LibertasMO-SFCC-28/152025-07-31
00810008128848LibertasMO-SFCC-28/162025-07-31
00810008128855LibertasMO-SFCC-28/172025-07-31
00810008128862LibertasMO-SFCC-28/182025-07-31
00810008128879LibertasMO-SFCC-28/202025-07-31
00810008128886LibertasMO-SFCC-28/222025-07-31
00810008128893LibertasMO-SFCC-28/242025-07-31
00810008129081LibertasMO-SFCC-32/042025-07-31
00810008129098LibertasMO-SFCC-32/052025-07-31
00810008129104LibertasMO-SFCC-32/062025-07-31
00810008129111LibertasMO-SFCC-32/072025-07-31

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Primary DI, Brand, Company table
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07613327014471ScorpioHowmedica Osteonics Corp.MBH2015-09-24
07613327014495ScorpioHowmedica Osteonics Corp.MBH2015-09-24
07613327014525ScorpioHowmedica Osteonics Corp.MBH2015-09-24
07613327014532ScorpioHowmedica Osteonics Corp.MBH2015-09-24