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VIKOS® Allograft System

FDA UDI

Class I (US FDA UDI)

by K2m, Inc.

Identity

Trade Name
VIKOS® Allograft System FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
Lordotic Rasp Size 14x14.5x5 mm, 7° FDA UDI
Model / Reference
PRO-1003-01 FDA UDI
Description
Lordotic Rasp Size 14x14.5x5 mm, 7° FDA UDI

Identifiers

Catalog Number
PRO-1003-01 FDA UDI
Primary DI / UDI-DI
10888857516908 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Dimensions & Sizes

Size
Width — 14.5 Millimeter FDA UDI
Depth — 14 Millimeter FDA UDI
Height — 5 Millimeter FDA UDI
Angle — 7 degree FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, reusable

VIKOS® Allograft System by K2m, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
K2m, Inc.

Sources (1)

  • FDA UDI b7832846-e90b-4854-b4d7-3639ed1c2f82 36 fields · synced Jun 1, 2026