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FDA 510(k)

CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT

K-Number: K924142 · 1993-06-15

ApplicantCodman & Shurtleff, Inc.
Decision Date1993-06-15
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT 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 1993-06-15 under 510(k) number K924142. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT?

CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K924142.

When did CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT receive FDA 510(k) clearance?

CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT received FDA 510(k) clearance on 1993-06-15, under 510(k) number K924142.

Who is the listed applicant for CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT?

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 CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT?

The FDA product code for CODMAN(TM) TITANIUM INTERLAMINAR CLAMP KIT is KWP.

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Related Devices (Code: KWP)

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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