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Maxan One Anterior Cervical Plate System 14-521650E2

by Biomet Spine LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888480591153 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Maxan One Anterior Cervical Plate System
Generic Name
Bone-screw internal spinal fixation system, sterile
Model / Ref / Catalog
14-521650E2
Primary DI / UDI-DI
00888480591153
FDA Product Code
KWQ
GMDN Term
Bone-screw internal spinal fixation system, sterile
Device Class
Class II
Regulation Number
888.3060
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone-screw internal spinal fixation system, sterile

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No