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Plexur P® 6000-425

by Medtronic Sofamor Danek, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number00613994986573 UDI-DI Date20 Jul 2015ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Plexur P®
Generic Name
Cadaveric-donor/synthetic polymer bone graft
Model / Reference
6000-425
Primary DI / UDI-DI
00613994986573
510(k) Number
FDA Product Code
MQV, MBP
GMDN Term
Cadaveric-donor/synthetic polymer bone graft
Device Class
Class II
Regulation Number
888.3045
GUDID distribution status
Not in Commercial Distribution
Size
Length — 25.0 Millimeter
Width — 50.0 Millimeter
Height — 4.0 Millimeter

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • HCT/P
  • Lot / Batch Number

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No