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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
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
Phantom ActivCore Nail, 10.0 X 200mm FDA UDI
Model / Reference
P31-102-2000-S FDA UDI
Description
Phantom ActivCore Nail, 10.0 X 200mm FDA UDI

Identifiers

Catalog Number
P31-102-2000-S FDA UDI
Primary DI / UDI-DI
00889795097712 FDA UDI
510(k) Number
K201227 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

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 Arthrodesis intramedullary nail, non-distracting.

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 f3ad8801-8b3f-4fef-9698-be7789349e5e 35 fields · synced Jun 8, 2026