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NextAR RSA Platform

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
NextAR RSA Platform FDA UDI
Generic Name
Optical surgical navigation device tracking system FDA UDI
Device Name
NextAR impaction handle FDA UDI
Model / Reference
04.01.10.0592 FDA UDI
Description
NextAR impaction handle FDA UDI

Identifiers

Primary DI / UDI-DI
07630345731180 FDA UDI
510(k) Number
K210153 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Optical surgical navigation device tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Optical surgical navigation device tracking system

NextAR RSA Platform by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Optical surgical navigation device tracking system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c727025d-b4a5-4395-a330-490993e5fe2e 34 fields · synced May 30, 2026