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Vitality® 07.02004.160

by Biomet Spine LLC

Vitality® 07.02004.160 is a Class II device made by Biomet Spine LLC, listed in FDA GUDID since 1 Dec 2015 (UDI-DI 00889024002739), 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 Number00889024002739 UDI-DI Date1 Dec 2015ListedStatusListed 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  • Withdrawn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
Vitality®
Generic name
Bone-screw internal spinal fixation system, non-sterile
Model / Ref / Catalog
07.02004.160
Primary DI / UDI-DI
00889024002739
FDA product code
NKB, OSH, KWP, MNI, MNH, KWQ
GMDN term
Bone-screw internal spinal fixation system, non-sterile
Device class
Class II
Regulation number
888.3070, 888.3050, 888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-screw internal spinal fixation system, non-sterile

Other devices from Biomet Spine LLC

See all devices from Biomet Spine LLC →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)