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FDA 510(k)

CODMAN SLIM-LOC SYSTEM

K-Number: K013877 · 2001-12-19

ApplicantCodman & Shurtleff, Inc.
Decision Date2001-12-19
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODMAN SLIM-LOC SYSTEM 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 2001-12-19 under 510(k) number K013877. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN SLIM-LOC SYSTEM?

CODMAN SLIM-LOC SYSTEM is a medical device that received FDA 510(k) clearance on 2001-12-19. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K013877.

When did CODMAN SLIM-LOC SYSTEM receive FDA 510(k) clearance?

CODMAN SLIM-LOC SYSTEM received FDA 510(k) clearance on 2001-12-19, under 510(k) number K013877.

Who is the listed applicant for CODMAN SLIM-LOC SYSTEM?

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 SLIM-LOC SYSTEM?

The FDA product code for CODMAN SLIM-LOC SYSTEM is KWQ.

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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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