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FDA 510(k)

SOLSTICE CROSS CONNECTOR

K-Number: K120998 · 2012-10-01

ApplicantLife Spine
Decision Date2012-10-01
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SOLSTICE CROSS CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine. It received FDA 510(k) clearance on 2012-10-01 under 510(k) number K120998. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLSTICE CROSS CONNECTOR?

SOLSTICE CROSS CONNECTOR is a medical device that received FDA 510(k) clearance on 2012-10-01. The listed applicant is Life Spine. The 510(k) number is K120998.

When did SOLSTICE CROSS CONNECTOR receive FDA 510(k) clearance?

SOLSTICE CROSS CONNECTOR received FDA 510(k) clearance on 2012-10-01, under 510(k) number K120998.

Who is the listed applicant for SOLSTICE CROSS CONNECTOR?

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

What is the FDA product code for SOLSTICE CROSS CONNECTOR?

The FDA product code for SOLSTICE CROSS CONNECTOR is KWP.

Related Clinical Trials

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.

Other records listing Life Spine 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 33 devices →

Related Devices (Code: KWP)

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.

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