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Phantom Hindfoot TTC/TC Nail System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
Phantom Hindfoot TTC/TC Nail System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Phantom Nail, Crossing Screw, Ø5.0mm x 75mm length, Headless FDA UDI
Model / Reference
P32-350-075F FDA UDI
Description
Phantom Nail, Crossing Screw, Ø5.0mm x 75mm length, Headless FDA UDI

Identifiers

Catalog Number
P32-350-075F FDA UDI
Primary DI / UDI-DI
00889795136473 FDA UDI
510(k) Number
K201227 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Phantom Hindfoot TTC/TC Nail System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 5723cad0-d73e-426f-98da-e4a88dfac08d 35 fields · synced Jun 8, 2026