FDA UDI In Commercial Distribution 🇺🇸 United States

MyKnee PPS

DI: 07630345772343 · Model: 28.2064S · Medacta International SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyKnee PPS
Primary DI
07630345772343
Version / Model
28.2064S
Company Name
Medacta International SA
Labeler DUNS
488227125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-01
Public Version
1
Public Version Date
2025-05-09
Public Version Status
New
Public Device Record Key
fad7653d-ef2e-4b60-a547-718ab60e313b

Device Description

MyKnee U STD FemPinPositioner-MRI-GMK-LL-#4 ST

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 07630345772343

Premarket Submissions

Submission Number Supplement Number
K170106 000