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Xlx

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
XLX FDA UDI
Generic Name
External spinal fixation system FDA UDI
Device Name
XLX ACR Attachment Tool, Implant FDA UDI
Model / Reference
1871540 FDA UDI
Description
XLX ACR Attachment Tool, Implant FDA UDI

Identifiers

Primary DI / UDI-DI
00887517944979 FDA UDI
510(k) Number
K173892 FDA UDI
FDA Product Code
OVD FDA UDI
MAX FDA UDI
PHM FDA UDI
GMDN Term
External spinal fixation system 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: External spinal fixation system

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

Similar devices

Also classified as External spinal fixation system.

Cleared under the same submission

K173892 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuvasive, Inc.

Sources (1)

  • FDA UDI bc19a5ce-40d2-4577-a00b-26664cd38b32 35 fields · synced Jun 8, 2026