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RIVA Posterior Fixation System FG1-52-095060

by Xenix Medical

Listed FDA GUDID listing, no authorization on record

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 Number00840493411422 UDI-DI Date9 Feb 2026ListedStatusListed GUDID: 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  • Withdrawn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
RIVA Posterior Fixation System
Generic name
Spinal bone screw, non-bioabsorbable
Model / Ref / Catalog
FG1-52-095060
Primary DI / UDI-DI
00840493411422
510(k) Number
FDA product code
NKB, KWQ, OLO
GMDN term
Spinal bone screw, non-bioabsorbable
Device class
Class II
Regulation number
888.3070, 888.3060, 882.4560
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Cleared under the same submission (K251154)

Show all (12)

Other devices from Xenix Medical

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Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Lot / batch number

Other properties (11)

  • Supplied 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