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FDA 510(k)

EVOL® -SI Joint Fusion System

K-Number: K190025 · 2019-08-12

Decision Date2019-08-12
Product CodeOUR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EVOL® -SI Joint Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is Cutting Edge Spine, LLC. It received FDA 510(k) clearance on 2019-08-12 under 510(k) number K190025. The device is classified under product code OUR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVOL® -SI Joint Fusion System?

EVOL® -SI Joint Fusion System is a medical device that received FDA 510(k) clearance on 2019-08-12. The listed applicant is Cutting Edge Spine, LLC. The 510(k) number is K190025.

When did EVOL® -SI Joint Fusion System receive FDA 510(k) clearance?

EVOL® -SI Joint Fusion System received FDA 510(k) clearance on 2019-08-12, under 510(k) number K190025.

Who is the listed applicant for EVOL® -SI Joint Fusion System?

The FDA 510(k) record lists Cutting Edge Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVOL® -SI Joint Fusion System?

The FDA product code for EVOL® -SI Joint Fusion System is OUR.

Other records listing Cutting Edge Spine, 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.

View all 9 devices →

Related Devices (Code: OUR)

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.