← Back to catalogue

Phantom® Fibula Nail System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
Phantom® Fibula Nail System FDA UDI
Generic Name
Bone nail end-cap FDA UDI
Device Name
5mm End Cap, Ti FDA UDI
Model / Reference
P36-503-0005 FDA UDI
Description
5mm End Cap, Ti FDA UDI

Identifiers

Catalog Number
P36-503-0005 FDA UDI
Primary DI / UDI-DI
00889795133311 FDA UDI
510(k) Number
K234128 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail end-cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone nail end-cap

Phantom® Fibula Nail System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 50590b9c-35c1-48e5-84d6-95293e8e9fd2 35 fields · synced May 30, 2026