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FDA 510(k)

SUNDT SLIM-LINE GRAFT CLIPS

K-Number: K912456 · 1995-03-10

Decision Date1995-03-10
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SUNDT SLIM-LINE GRAFT CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1995-03-10 under 510(k) number K912456. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNDT SLIM-LINE GRAFT CLIPS?

SUNDT SLIM-LINE GRAFT CLIPS is a medical device that received FDA 510(k) clearance on 1995-03-10. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K912456.

When did SUNDT SLIM-LINE GRAFT CLIPS receive FDA 510(k) clearance?

SUNDT SLIM-LINE GRAFT CLIPS received FDA 510(k) clearance on 1995-03-10, under 510(k) number K912456.

Who is the listed applicant for SUNDT SLIM-LINE GRAFT CLIPS?

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

What is the FDA product code for SUNDT SLIM-LINE GRAFT CLIPS?

The FDA product code for SUNDT SLIM-LINE GRAFT CLIPS is HCH.

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 Codman & Shurtleff, 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.

View all 147 devices →

Related Devices (Code: HCH)

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

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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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