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Gamma 3320-0320S

by Stryker Corp.

Gamma 3320-0320S is a Class II device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2015 (UDI-DI 07613153313229), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613153313229 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Gamma
Generic name
Femur intramedullary nail
Model / Ref / Catalog
3320-0320S
Primary DI / UDI-DI
07613153313229
FDA product code
HSB
GMDN term
Femur intramedullary nail
Device class
Class II
Regulation number
888.3020
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Length — 320.0 Millimeter
Angle — 120.0 degree

Related devices

Category: Femur intramedullary nail

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)