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Palladian™

FDA UDI

Class II (US FDA UDI)

by Neurostructures, Inc

Identity

Trade Name
Palladian™ FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
Curved Rod 45mm FDA UDI
Model / Reference
50-03-0045 FDA UDI
Description
Curved Rod 45mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841508102328 FDA UDI
FDA Product Code
NKB FDA UDI
KWP FDA UDI
MNI FDA UDI
MNH FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

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

Category: Bone-screw internal spinal fixation system, non-sterile

Palladian™ by Neurostructures, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neurostructures, Inc

Sources (1)

  • FDA UDI e5496902-cf85-45fd-8bb3-788ebbc35527 34 fields · synced Jun 8, 2026