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FDA 510(k)

SuRgical Planner (SRP)

K-Number: K170793 · 2018-02-12

ApplicantSurgical Theater, LLC
Decision Date2018-02-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SuRgical Planner (SRP) is a medical device manufactured by Surgical Theater, LLC. It received FDA 510(k) clearance on 2018-02-12 under approval number K170793. 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 SuRgical Planner (SRP)?

SuRgical Planner (SRP) is a medical device that received FDA 510(k) clearance on 2018-02-12. It is manufactured by Surgical Theater, LLC. The 510(k) number is K170793.

When was SuRgical Planner (SRP) approved by the FDA?

SuRgical Planner (SRP) received FDA 510(k) clearance on 2018-02-12, under approval number K170793.

What company makes SuRgical Planner (SRP)?

SuRgical Planner (SRP) is manufactured by Surgical Theater, LLC.

What is the FDA product code for SuRgical Planner (SRP)?

The FDA product code for SuRgical Planner (SRP) is LLZ.

Other Devices by Surgical Theater, LLC

K160584Surgical Navigation Advanced Platform (SNAP)

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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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