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Roll stand ACC00045

by Augmedics Ltd.

Roll stand ACC00045 is a multi-purpose stereotactic surgery system (FDA Class II; FDA product code SBF, Orthopedic Augmented Reality) made by Augmedics Ltd., cleared under FDA 510(k) K190929 on 20 Dec 2019 and listed in FDA GUDID since 16 Mar 2020 (UDI-DI 07290113780248), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K190929

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290113780248 UDI-DI Date16 Mar 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK190929 Date20 Dec 2019DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K190929 decided 20 Dec 2019 Active
  • FDA GUDID UDI-DI 07290113780248 listed 16 Mar 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K190929
  2. Listed FDA GUDID 07290113780248

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Roll stand
Generic name
Multi-purpose stereotactic surgery system
Model / reference
ACC00045
Primary DI / UDI-DI
07290113780248
510(k) Number
FDA product code
SBF
GMDN term
Multi-purpose stereotactic surgery system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Multi-purpose stereotactic surgery system.

Other devices from Augmedics Ltd.

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Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)