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Vitoss BA Injectable 2102-2301

by Stryker Orthobiologics

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 Number07613327064773 UDI-DI Date12 Jul 2017ListedStatusListed 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  • Withdrawn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
Vitoss BA Injectable
Generic Name
Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
Model / Ref / Catalog
2102-2301
Primary DI / UDI-DI
07613327064773
510(k) Number
FDA Product Code
MQV
GMDN Term
Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
Device Class
Class II
Regulation Number
888.3045
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone matrix implant, synthetic, non-antimicrobial

Cleared under the same submission (K163621)

Other devices from Stryker Orthobiologics

Properties

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

Other properties (9)

  • Contains Latex: 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