SurgicalPreview
K-Number: K171534 · 2017-11-08
ApplicantEndo Vantage, LLC
Decision Date2017-11-08
Product CodePZO
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
SurgicalPreview is a medical device manufactured by Endo Vantage, LLC. It received FDA 510(k) clearance on 2017-11-08 under approval number K171534. The device is classified under product code PZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SurgicalPreview?
SurgicalPreview is a medical device that received FDA 510(k) clearance on 2017-11-08. It is manufactured by Endo Vantage, LLC. The 510(k) number is K171534.
When was SurgicalPreview approved by the FDA?
SurgicalPreview received FDA 510(k) clearance on 2017-11-08, under approval number K171534.
What company makes SurgicalPreview?
SurgicalPreview is manufactured by Endo Vantage, LLC.
What is the FDA product code for SurgicalPreview?
The FDA product code for SurgicalPreview is PZO.
Related Devices (Code: PZO)
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.