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FDA 510(k)

SURGERY REHEARSAL PLATFORM

K-Number: K123023 · 2013-02-08

Decision Date2013-02-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SURGERY REHEARSAL PLATFORM is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Theater, LLC. It received FDA 510(k) clearance on 2013-02-08 under 510(k) number K123023. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGERY REHEARSAL PLATFORM?

SURGERY REHEARSAL PLATFORM is a medical device that received FDA 510(k) clearance on 2013-02-08. The listed applicant is Surgical Theater, LLC. The 510(k) number is K123023.

When did SURGERY REHEARSAL PLATFORM receive FDA 510(k) clearance?

SURGERY REHEARSAL PLATFORM received FDA 510(k) clearance on 2013-02-08, under 510(k) number K123023.

Who is the listed applicant for SURGERY REHEARSAL PLATFORM?

The FDA 510(k) record lists Surgical Theater, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGERY REHEARSAL PLATFORM?

The FDA product code for SURGERY REHEARSAL PLATFORM is LLZ.

Related Clinical Trials

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.

Other records listing Surgical Theater, LLC 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.

Related Devices (Code: LLZ)

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.

Official Source

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

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