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Xia I

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
XIA I FDA UDI
Generic Name
Bone-screw internal spinal fixation system connector FDA UDI
Device Name
CROSS LINK FDA UDI
Model / Reference
03803060 FDA UDI
Description
CROSS LINK FDA UDI

Identifiers

Catalog Number
03803060 FDA UDI
Primary DI / UDI-DI
04546540147929 FDA UDI
FDA Product Code
KWQ FDA UDI
NKB FDA UDI
KWP FDA UDI
MNI FDA UDI
MNH FDA UDI
GMDN Term
Bone-screw internal spinal fixation system connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 60.0 Millimeter FDA UDI

Xia I by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9388d612-8e44-4b3c-a8e3-7b4d23f1e007 36 fields · synced Jun 1, 2026