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Viper Prime 186775230S

by Medos International Sàrl GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10705034519715 UDI-DIDate8 Feb 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Viper Prime
Generic Name
Spinal bone screw, non-bioabsorbable
Model / Ref / Catalog
186775230S
Primary DI / UDI-DI
10705034519715
510(k) Number
FDA Product Code
KWQ, KWP, NKB
GMDN Term
Spinal bone screw, non-bioabsorbable
Device Class
Class II
Regulation Number
888.3060, 888.3050, 888.3070
GUDID distribution status
In Commercial Distribution

Related devices

Category: Spinal bone screw, non-bioabsorbable

Cleared under the same submission (K173095)

Show all (12)

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

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

Other properties (8)

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