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Inertia® Pedicle Screw and Deformity Correxxion® System 10-23-TRSM

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 Number00889929007730 UDI-DI Date21 Jul 2016ListedStatusListed 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  • Withdrawn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
Inertia® Pedicle Screw and Deformity Correxxion® System
Generic Name
Bone-screw internal spinal fixation system hook
Model / Reference
10-23-TRSM
Primary DI / UDI-DI
00889929007730
510(k) Number
FDA Product Code
MNH, MNI, KWP, NKB, OSH
GMDN Term
Bone-screw internal spinal fixation system hook
Device Class
Class II
Regulation Number
888.3070, 888.3050
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-screw internal spinal fixation system hook

Cleared under the same submission (K153453)

Show all (12)

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Properties

  • Single Use
  • Implantable
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • 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
  • Expiration Date: No
  • Manufacturing Date: No