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FDA 510(k)

Automatic Registration

K-Number: K234047 · 2024-03-20

ApplicantBrainlab AG
Decision Date2024-03-20
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Automatic Registration is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K234047. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Automatic Registration?

Automatic Registration is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Brainlab AG. The 510(k) number is K234047.

When did Automatic Registration receive FDA 510(k) clearance?

Automatic Registration received FDA 510(k) clearance on 2024-03-20, under 510(k) number K234047.

Who is the listed applicant for Automatic Registration?

The FDA 510(k) record lists Brainlab AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Automatic Registration?

The FDA product code for Automatic Registration is OLO.

Related Clinical Trials

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NCT05891002Accuracy of Robotically Assisted Cranial BiopsiesTERMINATED

Other records listing Brainlab AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: OLO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261410Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit))Suite 201, National Innovation CentreK261205SPINEART Navigation Instrument SystemSpineart SAK262121Ion-L Navigated InstrumentsSurGenTec, LLCK261024TMINI Miniature Robotic SystemTHINK Surgical, Inc.K261113Op.n™ Spine Navigation and Robotic GuidanceEcential RoboticsK261852OTS HipOrtoma AB

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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