AVS Anchor-C Cervical Cage System

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: AVS Anchor-C Cervical Cage System FDA UDI
Generic Name: Spinal implant trial FDA UDI
Device Name: TRIAL FDA UDI
Model / Reference: 48328708 FDA UDI
Description: TRIAL FDA UDI

Identifiers

Catalog Number: 48328708 FDA UDI
Primary DI / UDI-DI: 07613327267310 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Spinal implant trial 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

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Height — 10.0 Millimeter FDA UDI
Width — 14.0 Millimeter FDA UDI
Angle — 8.0 degree FDA UDI
Depth — 12.0 Millimeter FDA UDI

Category: Spinal implant trial

AVS Anchor-C Cervical Cage System by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 63feb959-6956-4025-96a5-f8fa082c7dd4 35 fields · synced May 31, 2026