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PathFinder NXT®

FDA UDI

Class II (US FDA UDI)

by Zimmer Spine, Inc.

Identity

Trade Name
PathFinder NXT® FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Model / Reference
3555-300 FDA UDI

Identifiers

Catalog Number
3555-300 FDA UDI
Primary DI / UDI-DI
00889024336278 FDA UDI
FDA Product Code
MNI FDA UDI
NKB FDA UDI
MNH FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

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

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Spine, Inc.

Sources (1)

  • FDA UDI 7eb713c0-3d75-4056-a6b6-19c68be58662 34 fields · synced Jun 8, 2026