Pathfinder NXT

FDA UDI

Class II (US FDA UDI)

by Zimmer Spine, Inc.

Identity

Trade Name: Pathfinder NXT FDA UDI
Generic Name: Bone tap, reusable FDA UDI
Device Name: PathFinder NXT® PAT Tap, 5.0mm FDA UDI
Model / Reference: 07.00777.702 FDA UDI
Description: PathFinder NXT® PAT Tap, 5.0mm FDA UDI

Identifiers

Catalog Number: 07.00777.702 FDA UDI
Primary DI / UDI-DI: 00880304989405 FDA UDI
FDA Product Code: NKB FDA UDI
GMDN Term: Bone tap, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 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

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: Bone tap, reusable

Pathfinder NXT by Zimmer Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

BIOSURE — Smith & Nephew, Inc. · Class I
NobelActive® — Nobel Biocare AG · Class I
CORTICAL TAP — Biomet Orthopedics, Inc. · Class I
PressON™ — NEXUS SPINE, L.L.C. · Class I
Insite — TORNIER, INC. · Class I
ReLine — Nuvasive, Inc. · Class I
Mariner MIS — SeaSpine Orthopedics Corporation · Class I
Response 5.5/6.0 Spine System — ORTHOPEDIATRICS CORP. · Class I

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

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

Manufacturer

Manufacturer: Zimmer Spine, Inc.

Sources (1)

FDA UDI 5b44eb22-415d-4177-9c9c-37d8a672383a 36 fields · synced May 30, 2026