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Matrixx System 55M-26L-09-SP

by Nexxt Spine LLC

Listed FDA GUDID listing, no authorization on record

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 Number00889929067062 UDI-DI Date26 Mar 2025ListedStatusListed GUDID: 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  • Withdrawn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
Matrixx System
Generic Name
Metallic spinal interbody fusion cage
Model / Reference
55M-26L-09-SP
Primary DI / UDI-DI
00889929067062
510(k) Number
FDA Product Code
MQP
GMDN Term
Metallic spinal interbody fusion cage
Device Class
Class II
Regulation Number
888.3060
GUDID distribution status
In Commercial Distribution
Size
Length — 26 Millimeter
Width — 9 Millimeter
Height — 9 Millimeter
Angle — 6 degree

Related devices

Category: Metallic spinal interbody fusion cage

Cleared under the same submission (K171140)

Show all (12)

Other devices from Nexxt Spine LLC

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Properties

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

Other properties (9)

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