Skip to content

Pathfinder NXT 07.00777.702

by Zimmer Spine, Inc.

Pathfinder NXT 07.00777.702 is a Class II device made by Zimmer Spine, Inc., listed in FDA GUDID since 30 May 2017 (UDI-DI 00880304989405), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304989405 UDI-DI Date30 May 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pathfinder NXT
Generic name
Bone tap, reusable
Model / Ref / Catalog
07.00777.702
Primary DI / UDI-DI
00880304989405
FDA product code
NKB
GMDN term
Bone tap, reusable
Device class
Class II
Regulation number
888.3070
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

Other devices from Zimmer Spine, Inc.

See all devices from Zimmer Spine, Inc. →

Properties

  • Sterilise before use
  • Lot / batch number
Other properties (13, all answered No)