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Citadel

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
CITADEL FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
CITADEL Anterior Lumbar Plate, 1-Level, 38mm FDA UDI
Model / Reference
130.138 FDA UDI
Description
CITADEL Anterior Lumbar Plate, 1-Level, 38mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889095038866 FDA UDI
510(k) Number
K062836 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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
Length — 38 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

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

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7850c4b6-8469-418f-856b-072402a86a38 36 fields · synced Jun 8, 2026