Base

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name: BASE FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: BASE Ti Implant, 8x34x24mm 10° FDA UDI
Model / Reference: 6951810 FDA UDI
Description: BASE Ti Implant, 8x34x24mm 10° FDA UDI

Identifiers

Primary DI / UDI-DI: 00887517700810 FDA UDI
510(k) Number: K151214 FDA UDI
K170592 FDA UDI
FDA Product Code: OVD FDA UDI
GMDN Term: Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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: Metallic spinal interbody fusion cage

The BASE Ti Implant is a cutting-edge, metallic spinal interbody fusion cage designed to provide mechanical stability and promote bone fusion between two contiguous vertebral bodies. Featuring a hollow, porous design, this implant is used in the treatment of degenerative disc disease (DDD) and is typically packaged with fixation screws and devices for optimal patient outcomes.

Similar devices

Also classified as Metallic spinal interbody fusion cage.

KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
MectaLIF 3D — Medacta International · Class II
PILLAR TL — Orthofix US LLC · Class II
Solar™ Interbody Fusion System — Degen Medical · Class II
Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
ShurFit Lumbar Interbody — Precision Spine, Inc. · Class II

Cleared under the same submission

K151214 also covers:

K170592 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Nuvasive, Inc.

Sources (1)

FDA UDI 954c8bd5-ea23-4d04-964f-cdd37bab70da 35 fields · synced Jul 14, 2026