Reliance Buttress Washer System

FDA UDI

Class II (US FDA UDI)

by Vy Spine Llc

Identity

Trade Name: Reliance Buttress Washer System FDA UDI
Generic Name: Metallic spinal fusion cage, non-sterile FDA UDI
Device Name: Buttress Washer-Narrow, 20mm FDA UDI
Model / Reference: 8-01-020 FDA UDI
Description: Buttress Washer-Narrow, 20mm FDA UDI

Identifiers

Catalog Number: 8-01-020 FDA UDI
Primary DI / UDI-DI: 00842566106938 FDA UDI
510(k) Number: K073349 FDA UDI
FDA Product Code: KWQ FDA UDI
GMDN Term: Metallic spinal fusion cage, non-sterile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Metallic spinal fusion cage, non-sterile

Reliance Buttress Washer System by Vy Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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IVA Cage Ti — Dio Medical Co., Ltd. · Class II

Cleared under the same submission

K073349 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Vy Spine Llc

Sources (1)

FDA UDI b0d13c5f-e57e-428f-94bf-4c0144669ae8 36 fields · synced May 31, 2026