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Galaxy Fixation System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
Galaxy Fixation System FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
GALAXY SMALL SPANNING 'Z' FRAME STERILE KIT FDA UDI
Model / Reference
1 FDA UDI
Description
GALAXY SMALL SPANNING 'Z' FRAME STERILE KIT FDA UDI

Identifiers

Catalog Number
99-93498 FDA UDI
Primary DI / UDI-DI
18054242515197 FDA UDI
510(k) Number
K141760 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: External orthopaedic fixation system, single-use

Galaxy Fixation System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI dacbd25d-c881-405d-8c1a-d8a3d267fcba 36 fields · synced Jun 1, 2026