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FDA 510(k)

DUOCLIPPER TITANIUM CLIPS

K-Number: K973652 · 1998-03-27

ApplicantScion International, Inc.
Decision Date1998-03-27
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DUOCLIPPER TITANIUM CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Scion International, Inc.. It received FDA 510(k) clearance on 1998-03-27 under 510(k) number K973652. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOCLIPPER TITANIUM CLIPS?

DUOCLIPPER TITANIUM CLIPS is a medical device that received FDA 510(k) clearance on 1998-03-27. The listed applicant is Scion International, Inc.. The 510(k) number is K973652.

When did DUOCLIPPER TITANIUM CLIPS receive FDA 510(k) clearance?

DUOCLIPPER TITANIUM CLIPS received FDA 510(k) clearance on 1998-03-27, under 510(k) number K973652.

Who is the listed applicant for DUOCLIPPER TITANIUM CLIPS?

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

What is the FDA product code for DUOCLIPPER TITANIUM CLIPS?

The FDA product code for DUOCLIPPER TITANIUM CLIPS is FZP.

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Other records listing Scion International, Inc. 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.

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Related Devices (Code: FZP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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