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WayPoint™ Combination Driver Bit

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
WayPoint™ Combination Driver Bit FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
WayPoint Combination Driver Bit with Collar FDA UDI
Model / Reference
66-WP-CD-01-00320 FDA UDI
Description
WayPoint Combination Driver Bit with Collar FDA UDI

Identifiers

Catalog Number
66-WP-CD-01 FDA UDI
Primary DI / UDI-DI
00873263003206 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neurological stereotactic surgery system

WayPoint™ Combination Driver Bit 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 a89b75be-9161-47cf-8fd2-e4b0170818d3 36 fields · synced Jun 1, 2026