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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 POLYAXIAL SCREW 4.5 x 5.0 x 55mm FDA UDI
Model / Reference
186212555 FDA UDI
Description
EXPEDIUM SPINE SYSTEM POLYAXIAL SCREW 4.5 x 5.0 x 55mm FDA UDI

Identifiers

Catalog Number
186212555 FDA UDI
Primary DI / UDI-DI
10705034112398 FDA UDI
510(k) Number
K073364 FDA UDI
K111136 FDA UDI
FDA Product Code
KWP FDA UDI
OSH FDA UDI
MNH FDA UDI
MNI FDA UDI
KWQ FDA UDI
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3070 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

K073364 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 53f8f6da-c237-49e4-9713-c828bda809fc 37 fields · synced May 31, 2026