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Daytona 97-6489

by SeaSpine Orthopedics Corporation

Daytona 97-6489 is a Class I device made by SeaSpine Orthopedics Corporation, listed in FDA GUDID since 21 Mar 2017 (UDI-DI 10889981139605), 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 Number10889981139605 UDI-DI Date21 Mar 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  • Withdrawn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
Daytona
Generic name
Orthopaedic implant driver
Model / Ref / Catalog
97-6489
Primary DI / UDI-DI
10889981139605
FDA product code
HXX
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant driver

Similar devices in this category

Other devices filed under Orthopaedic implant driver.

Other devices from SeaSpine Orthopedics Corporation

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)