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Firebird

FDA UDI

Class II (US FDA UDI)

by Orthofix US LLC

Identity

Trade Name
FIREBIRD FDA UDI
Generic Name
Bone-screw internal spinal fixation system FDA UDI
Device Name
45mm Multi-Axial Cross-Connector FDA UDI
Model / Reference
55-5345 FDA UDI
Description
45mm Multi-Axial Cross-Connector FDA UDI

Identifiers

Primary DI / UDI-DI
18257200016365 FDA UDI
510(k) Number
K122901 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
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

Dimensions & Sizes

Size
Length — 45 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system

Firebird by Orthofix US LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix US LLC

Sources (1)

  • FDA UDI 61e51da2-b523-42e5-8b35-eb1faaf2082a 36 fields · synced Jun 8, 2026