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Sequoia® 3360-065

by Zimmer Spine, Inc.

Sequoia® 3360-065 is a Class II device made by Zimmer Spine, Inc., listed in FDA GUDID since 23 Jun 2016 (UDI-DI 00889024335455), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024335455 UDI-DI Date23 Jun 2016ListedStatusListed 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  • Withdrawn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
Sequoia®
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
3360-065
Primary DI / UDI-DI
00889024335455
FDA product code
MNI, NKB, MNH
GMDN term
Orthopaedic surgical procedure kit, non-medicated, 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: Orthopaedic surgical procedure kit, non-medicated, reusable

Similar devices in this category

Other devices filed under Orthopaedic surgical procedure kit, non-medicated, reusable.

Other devices from Zimmer Spine, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)