SuRgical Planner (SRP)
K-Number: K170793 · 2018-02-12
Device Summary
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. The listed applicant is Surgical Theater, LLC. The 510(k) number is K170793.
When did SuRgical Planner (SRP) receive FDA 510(k) clearance?
SuRgical Planner (SRP) received FDA 510(k) clearance on 2018-02-12, under 510(k) number K170793.
Who is the listed applicant for SuRgical Planner (SRP)?
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 SuRgical Planner (SRP)?
The FDA product code for SuRgical Planner (SRP) is LLZ.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.