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SpineMap Go 81-81041

by Stryker Leibinger

SpineMap Go 81-81041 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 12 Apr 2019 (UDI-DI 07613327413007), 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 Number07613327413007 UDI-DI Date12 Apr 2019ListedStatusListed 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  • Withdrawn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
SpineMap Go
Generic name
Surgical planning/navigation-enhancement system
Model / Ref / Catalog
81-81041
Primary DI / UDI-DI
07613327413007
FDA product code
OLO
GMDN term
Surgical planning/navigation-enhancement system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical planning/navigation-enhancement system

Similar devices in this category

Other devices filed under Surgical planning/navigation-enhancement system.

Other devices from Stryker Leibinger

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  • 92-55771

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  • 92-55770

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See all devices from Stryker Leibinger →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)