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ClearPoint

FDA UDI

Class II (US FDA UDI)

by Clearpoint Neuro, Inc.

Identity

Trade Name
ClearPoint FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
ClearPoint Fixation Frame Screws, Philips FDA UDI
Model / Reference
CP-FFS-02 FDA UDI
Description
ClearPoint Fixation Frame Screws, Philips FDA UDI

Identifiers

Catalog Number
CP-FFS-02 FDA UDI
Primary DI / UDI-DI
00850376007352 FDA UDI
510(k) Number
K091439 FDA UDI
FDA Product Code
HBL FDA UDI
GMDN Term
Skull clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4460 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

Yes

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Skull clamp

ClearPoint by Clearpoint Neuro, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skull clamp.

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 c0132098-e1de-4b5c-ae88-bbee7f47f989 36 fields · synced May 30, 2026