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Coalition

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
COALITION FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
COALITION Spacer, 12mm x 14mm, 7deg, 8mm FDA UDI
Model / Reference
384.108 FDA UDI
Description
COALITION Spacer, 12mm x 14mm, 7deg, 8mm FDA UDI

Identifiers

Primary DI / UDI-DI
00849044027341 FDA UDI
FDA Product Code
OVE FDA UDI
ODP 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Dimensions & Sizes

Size
Depth — 12 Millimeter FDA UDI
Height — 8 Millimeter FDA UDI
Width — 14 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Coalition by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01e3dc01-2e0e-417e-90e4-f0ee8cddb1c0 35 fields · synced May 31, 2026