Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Parcus SLiK Anchors

K-Number: K170327 · 2017-03-30

Decision Date2017-03-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Parcus SLiK Anchors is a medical device manufactured by Parcus Medical. It received FDA 510(k) clearance on 2017-03-30 under approval number K170327. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Parcus SLiK Anchors?

Parcus SLiK Anchors is a medical device that received FDA 510(k) clearance on 2017-03-30. It is manufactured by Parcus Medical. The 510(k) number is K170327.

When was Parcus SLiK Anchors approved by the FDA?

Parcus SLiK Anchors received FDA 510(k) clearance on 2017-03-30, under approval number K170327.

What company makes Parcus SLiK Anchors?

Parcus SLiK Anchors is manufactured by Parcus Medical.

What is the FDA product code for Parcus SLiK Anchors?

The FDA product code for Parcus SLiK Anchors is MBI.

Other Devices by Parcus Medical

Related Devices (Code: MBI)

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.