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Expedium

FDA UDI

Class II (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
EXPEDIUM FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
EXPEDIUM SPINE SYSTEM STRAIGHT NUT 4.5 FDA UDI
Model / Reference
186200003 FDA UDI
Description
EXPEDIUM SPINE SYSTEM STRAIGHT NUT 4.5 FDA UDI

Identifiers

Catalog Number
186200003 FDA UDI
Primary DI / UDI-DI
10705034111070 FDA UDI
510(k) Number
K081252 FDA UDI
K111136 FDA UDI
FDA Product Code
OSH FDA UDI
MNH FDA UDI
NKB FDA UDI
MNI FDA UDI
KWP FDA UDI
KWQ FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Expedium by Depuy Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K081252 also covers:

K111136 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Spine, Inc.

Sources (1)

  • FDA UDI 6351baca-9324-42e6-aa00-69a9bbff2765 37 fields · synced May 31, 2026