← Back to catalogue

Anteralign Spinal System with Titan nanoLock Surface technology

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Anteralign Spinal System with Titan nanoLock Surface technology FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
SPACER 46501218 SM TI 12DG 32X25X18MM FDA UDI
Model / Reference
46501218 FDA UDI
Description
SPACER 46501218 SM TI 12DG 32X25X18MM FDA UDI

Identifiers

Primary DI / UDI-DI
00763000129781 FDA UDI
510(k) Number
K214010 FDA UDI
FDA Product Code
MAX FDA UDI
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

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Metallic spinal interbody fusion cage

Anteralign Spinal System with Titan nanoLock Surface technology by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI f9606540-20b8-4f24-9cf3-43c5df75006a 35 fields · synced May 30, 2026