Conquest Fn

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: CONQUEST FN FDA UDI
Generic Name: Bone tap, reusable FDA UDI
Device Name: CONQUEST FN PROXIMAL SCREW TAP - COMPRESSION FDA UDI
Model / Reference: 71179209 FDA UDI
Description: CONQUEST FN PROXIMAL SCREW TAP - COMPRESSION FDA UDI

Identifiers

Catalog Number: 71179209 FDA UDI
Primary DI / UDI-DI: 00885556533147 FDA UDI
510(k) Number: K152686 FDA UDI
FDA Product Code: KTT FDA UDI
JDO FDA UDI
GMDN Term: Bone tap, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Bone tap, reusable

Conquest Fn by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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ReLine — Nuvasive, Inc. · Class I
Mariner MIS — SeaSpine Orthopedics Corporation · Class I
Response 5.5/6.0 Spine System — ORTHOPEDIATRICS CORP. · Class I
Nautilus Spinal System — Life Spine, Inc. · Class II

Cleared under the same submission

K152686 also covers:

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: Smith & Nephew, Inc.

Sources (1)

FDA UDI c32fa1c9-44db-4b17-8ee8-dc5110400697 36 fields · synced Jun 8, 2026