X-Core

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name: X-CORE FDA UDI
Generic Name: Vertebral body prosthesis FDA UDI
Device Name: XC Mini Endcap, 15x12mm Parallel Ø12 FDA UDI
Model / Reference: 5962520 FDA UDI
Description: XC Mini Endcap, 15x12mm Parallel Ø12 FDA UDI

Identifiers

Primary DI / UDI-DI: 00887517269966 FDA UDI
510(k) Number: K090176 FDA UDI
K142205 FDA UDI
K151651 FDA UDI
FDA Product Code: MQP FDA UDI
PLT FDA UDI
GMDN Term: Vertebral body prosthesis 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

FDA UDI

Implantable

Yes

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

Category: Vertebral body prosthesis

X-Core by Nuvasive, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral body prosthesis.

CASCADIA™ Interbody System — K2M, INC. · Class II
CHESAPEAKE® Stabilization System — K2M, INC. · Class II
CASCADIA™ Interbody System — K2M, INC. · Class II
FORTIFY — GLOBUS MEDICAL, INC. · Class II
VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
CASCADIA™ Interbody System — K2M, INC. · Class II
CAPRI™ Corpectomy Cage System — K2M, INC. · Class II
Cascadia™ Interbody System — K2M, INC. · Class II

Cleared under the same submission

K090176 also covers:

K142205 also covers:

K151651 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: Nuvasive, Inc.

Sources (1)

FDA UDI 2cc3542f-34e9-47df-9234-d841f414ed36 35 fields · synced May 30, 2026