My Knee Femoral Cutting Blocks

Primary DI
07630030847868
Brand
My Knee Femoral Cutting Blocks
Company
Medacta International SA
Model
4.1011S
Device description
CT Left Medial #1 Sterile
Published
2014-11-18
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
OOGKnee Arthroplasty Implantation System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerOrthopedic2
OOGKnee Arthroplasty Implantation SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K093806000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K093806000MYKNEE CUTTING BLOCKSMedacta International S.A.2010-04-08JWH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07630030847868PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07630030847868076300308478687630030847868

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation instrument, single-useA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
488227125
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07630345700551NextAR TSA Platform5.3KSWNXAR2026-07-10
07630345729316NextAR TSA Platform5.3SSWNXAR2026-04-13
07630345728975Navigation System for Knee surgery33.22.10002026-01-26
07630699701792Navigation System for Knee surgery33.22.1000US2026-01-26
07630345725912NextAR Spine Platform98.46.NEXTAR2026-01-20
07630542722332NextAR Hip Platform09.23.10.IMU2026-01-14
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07630542759130NextAR™ Spine03.57.10.02622025-11-14
07630542759147NextAR™ Spine03.57.10.02632025-11-14
07630542720390NextAR Spine Platform03.57.10.02032025-09-19
07630542720406NextAR Spine Platform03.57.10.02042025-09-19
07630542720413NextAR Spine Platform03.57.10.02052025-09-19
07630542720420NextAR Spine Platform03.57.10.02062025-09-19
07630542720437NextAR Spine Platform03.57.10.02072025-09-19
07630542720444NextAR Spine Platform03.57.10.02082025-09-19
07630542720451NextAR Spine Platform03.57.10.02092025-09-19
07630542765346NextAR (TM) Shoulder Platform04.01.10.09022025-09-17
07630542765353NextAR (TM) Shoulder Platform04.01.10.09032025-09-17
07630542765360NextAR (TM) Shoulder Platform04.01.10.09042025-09-17
07630542765421NextAR (TM) Shoulder Platform04.01.10.09102025-09-17

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