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WayPoint™ Navigator

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
WayPoint™ Navigator FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
WayPoint ™ Navigator - Starter License FDA UDI
Model / Reference
C0239-00782 FDA UDI
Description
WayPoint ™ Navigator - Starter License FDA UDI

Identifiers

Catalog Number
C0239 FDA UDI
Primary DI / UDI-DI
00873263007822 FDA UDI
510(k) Number
K092192 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurological stereotactic surgery 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neurological stereotactic surgery system

WayPoint™ Navigator by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI db15e460-8c7f-4c0a-9878-4dacb0453f24 36 fields · synced May 30, 2026