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CD HORIZON® Spinal System

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
CD HORIZON® Spinal System FDA UDI
Generic Name
Scalpel handle, reusable FDA UDI
Device Name
HANDLE RBT030003 RG 5.5/6.0 SCALPEL LONG FDA UDI
Model / Reference
RBT030003 FDA UDI
Description
HANDLE RBT030003 RG 5.5/6.0 SCALPEL LONG FDA UDI

Identifiers

Primary DI / UDI-DI
00763000140410 FDA UDI
510(k) Number
K182121 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Scalpel handle, reusable 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Scalpel handle, reusable

CD HORIZON® Spinal System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel handle, reusable.

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 5381f58e-7406-466a-b32a-65d2c743b6b3 35 fields · synced Jun 1, 2026