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Fitbone® TAA0960-F-220

by Wittenstein Intens GmbH GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04260170142375 UDI-DIDate17 Apr 2021ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Fitbone®
Generic Name
Long bone distraction intramedullary nail, motorized
Model / Ref / Catalog
TAA0960-F-220, 60001764
Primary DI / UDI-DI
04260170142375
FDA Product Code
HSB
GMDN Term
Long bone distraction intramedullary nail, motorized
Device Class
Class II
Regulation Number
888.3020
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe
Size
Outer Diameter — 9 Millimeter
Length — 220 Millimeter

Other devices from Wittenstein Intens GmbH

  • Fitbone Taa

    Class II

  • Fitbone(R) Taa

    Class II

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No