FDA UDI In Commercial Distribution 🇺🇸 United States

MyPAO

DI: 07630542724428 · Model: 12.1032 · Medacta International SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyPAO
Primary DI
07630542724428
Version / Model
12.1032
Company Name
Medacta International SA
Labeler DUNS
488227125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-05
Public Version
1
Public Version Date
2025-12-15
Public Version Status
New
Public Device Record Key
c6190fa1-ce22-46b8-a11b-1e12804ac48e

Device Description

MyPAO Realignment Guide SA Right

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
PBF Orthopaedic Surgical Planning And Instrument Guides

GMDN Terms

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

Identifiers

Type ID
Primary 07630542724428

Premarket Submissions

Submission Number Supplement Number
K242603 000