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FDA 510(k)

SFX SNAP-FIT CROSS CONNECTOR

K-Number: K062196 · 2006-09-11

ApplicantDepuy Spine, Inc.
Decision Date2006-09-11
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SFX SNAP-FIT CROSS CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Spine, Inc.. It received FDA 510(k) clearance on 2006-09-11 under 510(k) number K062196. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SFX SNAP-FIT CROSS CONNECTOR?

SFX SNAP-FIT CROSS CONNECTOR is a medical device that received FDA 510(k) clearance on 2006-09-11. The listed applicant is Depuy Spine, Inc.. The 510(k) number is K062196.

When did SFX SNAP-FIT CROSS CONNECTOR receive FDA 510(k) clearance?

SFX SNAP-FIT CROSS CONNECTOR received FDA 510(k) clearance on 2006-09-11, under 510(k) number K062196.

Who is the listed applicant for SFX SNAP-FIT CROSS CONNECTOR?

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

What is the FDA product code for SFX SNAP-FIT CROSS CONNECTOR?

The FDA product code for SFX SNAP-FIT CROSS CONNECTOR is MNH. This falls under the ENT category.

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Other records listing Depuy Spine, Inc. as applicant

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Related Devices (Code: MNH)

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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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