← Back to catalogue

MyPAO Planning report

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
MyPAO Planning report FDA UDI
Generic Name
Orthopaedic/craniofacial implantation planning software FDA UDI
Device Name
MyPAO Planning report FDA UDI
Model / Reference
05.07.001SWO FDA UDI
Description
MyPAO Planning report FDA UDI

Identifiers

Primary DI / UDI-DI
07630971243378 FDA UDI
510(k) Number
K200589 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Orthopaedic/craniofacial implantation planning software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic/craniofacial implantation planning software

MyPAO Planning report by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic/craniofacial implantation planning software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medacta International

Sources (1)

  • FDA UDI 65c7d536-cbab-4cce-bbc3-7556c33722ba 34 fields · synced May 30, 2026