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FDA 510(k)

CAYMAN BUTTRESS PLATE SYSTEM

K-Number: K080302 · 2008-03-24

ApplicantK2m, Inc.
Decision Date2008-03-24
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAYMAN BUTTRESS PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is K2m, Inc.. It received FDA 510(k) clearance on 2008-03-24 under 510(k) number K080302. 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 CAYMAN BUTTRESS PLATE SYSTEM?

CAYMAN BUTTRESS PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-24. The listed applicant is K2m, Inc.. The 510(k) number is K080302.

When did CAYMAN BUTTRESS PLATE SYSTEM receive FDA 510(k) clearance?

CAYMAN BUTTRESS PLATE SYSTEM received FDA 510(k) clearance on 2008-03-24, under 510(k) number K080302.

Who is the listed applicant for CAYMAN BUTTRESS PLATE SYSTEM?

The FDA 510(k) record lists K2m, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAYMAN BUTTRESS PLATE SYSTEM?

The FDA product code for CAYMAN BUTTRESS PLATE SYSTEM is KWQ.

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Related Devices (Code: 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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