SUNDT SLIM-LINE GRAFT CLIPS
K-Number: K912456 · 1995-03-10
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Device Summary
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.
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
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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