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FDA 510(k)

StealthStation Spinous Process Clamps

K-Number: K211442 · 2021-07-08

Decision Date2021-07-08
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

StealthStation Spinous Process Clamps is a medical device manufactured by Medtronic Navigation. It received FDA 510(k) clearance on 2021-07-08 under approval number K211442. 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 StealthStation Spinous Process Clamps?

StealthStation Spinous Process Clamps is a medical device that received FDA 510(k) clearance on 2021-07-08. It is manufactured by Medtronic Navigation. The 510(k) number is K211442.

When was StealthStation Spinous Process Clamps approved by the FDA?

StealthStation Spinous Process Clamps received FDA 510(k) clearance on 2021-07-08, under approval number K211442.

What company makes StealthStation Spinous Process Clamps?

StealthStation Spinous Process Clamps is manufactured by Medtronic Navigation.

What is the FDA product code for StealthStation Spinous Process Clamps?

The FDA product code for StealthStation Spinous Process Clamps is OLO.

Other Devices by Medtronic Navigation

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Related Devices (Code: OLO)

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.