Piccolo Composite Nailing System

FDA UDI

Class II (US FDA UDI)

by Carbofix Orthopedics Ltd

Identity

Trade Name: Piccolo Composite Nailing System FDA UDI
Generic Name: Orthopaedic implantation hammering attachment FDA UDI
Device Name: Striking Adapter for use with the Piccolo Composite Proximal Femur Nailing System. FDA UDI
Model / Reference: Striking Adapter FDA UDI
Description: Striking Adapter for use with the Piccolo Composite Proximal Femur Nailing System. FDA UDI

Identifiers

Catalog Number: PPF910510 FDA UDI
Primary DI / UDI-DI: 07290109337999 FDA UDI
510(k) Number: K151010 FDA UDI
K153536 FDA UDI
FDA Product Code: HSB FDA UDI
GMDN Term: Orthopaedic implantation hammering attachment 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation hammering attachment

Piccolo Composite Nailing System by Carbofix Orthopedics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Carbofix Orthopedics Ltd

Sources (1)

FDA UDI f5e94602-e2bd-4ac8-abe0-3973ac7d4cf8 36 fields · synced Jun 1, 2026