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Plexur P® 60000109

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 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169218208 UDI-DI Date20 Jul 2015ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 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  • Withdrawn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
60000109
Primary DI / UDI-DI
00643169218208
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
MRI Safety
MR Safe
Size
Width — 25.0 Millimeter
Length — 9.0 Millimeter

Related devices

Cleared under the same submission (K080511)

Other devices from Medtronic Sofamor Danek, Inc.

See all devices from Medtronic Sofamor Danek, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • HCT/P
  • Serial Number

Other properties (8)

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