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Instrument Adapter, Starlock Interface 55080D

by Brainlab SE

Instrument Adapter, Starlock Interface 55080D is a Class II device made by Brainlab SE, cleared under FDA 510(k) K102990 on 4 Apr 2011 and listed in FDA GUDID since 15 Sep 2016 (UDI-DI 04056481001650), active (FDA 510(k)), not in commercial distribution (GUDID) as of 23 Oct 2026. One FDA recall is linked to it.

Active United States. Also listed in GUDID (US), not in commercial distribution.

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

510(k) K102990

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04056481001650 UDI-DI Date15 Sep 2016ListedStatusListed GUDID: not in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK102990 Date4 Apr 2011DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K102990 decided 4 Apr 2011 Active
  • FDA GUDID UDI-DI 04056481001650 listed 15 Sep 2016 Listed

Recalls

1 recall · FDA

    • Terminated Z-0959-2017 FDA Class II initiated 27 Oct 2016

    Brainlab Knee Navigation System: Femoral and Tibial Cutting Block Adapter Base with specific serial numbers might contain parts made from incorrect material and therefore not be suitable for reprocessing

Timeline

3 dated events

  1. Cleared FDA 510(k) K102990
  2. Listed FDA GUDID 04056481001650
  3. Recall initiated FDA recalls Z-0959-2017

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Instrument Adapter, Starlock Interface
Generic name
Robotic surgical navigation system
Model / Ref / Catalog
55080D
Primary DI / UDI-DI
04056481001650
510(k) Number
FDA product code
OLO
GMDN term
Robotic surgical navigation system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Cleared under the same submission (K102990)

Similar devices

Other devices filed under FDA product code OLO (Orthopedic Stereotaxic Instrument).

Other devices from Brainlab SE

See all devices from Brainlab SE →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)