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FDA 510(k)

END-TO-END AND SIDE-BY-SIDE CONNECTORS

K-Number: K010563 · 2001-05-25

ApplicantSpinal Concepts, Inc.
Decision Date2001-05-25
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

END-TO-END AND SIDE-BY-SIDE CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Concepts, Inc.. It received FDA 510(k) clearance on 2001-05-25 under 510(k) number K010563. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the END-TO-END AND SIDE-BY-SIDE CONNECTORS?

END-TO-END AND SIDE-BY-SIDE CONNECTORS is a medical device that received FDA 510(k) clearance on 2001-05-25. The listed applicant is Spinal Concepts, Inc.. The 510(k) number is K010563.

When did END-TO-END AND SIDE-BY-SIDE CONNECTORS receive FDA 510(k) clearance?

END-TO-END AND SIDE-BY-SIDE CONNECTORS received FDA 510(k) clearance on 2001-05-25, under 510(k) number K010563.

Who is the listed applicant for END-TO-END AND SIDE-BY-SIDE CONNECTORS?

The FDA 510(k) record lists Spinal Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for END-TO-END AND SIDE-BY-SIDE CONNECTORS?

The FDA product code for END-TO-END AND SIDE-BY-SIDE CONNECTORS is MNI.

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Other records listing Spinal Concepts, Inc. as applicant

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Related Devices (Code: MNI)

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.

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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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