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FDA 510(k)

COMPRESSION STAPLE AND SIMPLE STAPLE

K-Number: K043059 · 2005-01-18

ApplicantWrightmedicaltechnologyinc
Decision Date2005-01-18
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPRESSION STAPLE AND SIMPLE STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2005-01-18 under 510(k) number K043059. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSION STAPLE AND SIMPLE STAPLE?

COMPRESSION STAPLE AND SIMPLE STAPLE is a medical device that received FDA 510(k) clearance on 2005-01-18. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K043059.

When did COMPRESSION STAPLE AND SIMPLE STAPLE receive FDA 510(k) clearance?

COMPRESSION STAPLE AND SIMPLE STAPLE received FDA 510(k) clearance on 2005-01-18, under 510(k) number K043059.

Who is the listed applicant for COMPRESSION STAPLE AND SIMPLE STAPLE?

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

What is the FDA product code for COMPRESSION STAPLE AND SIMPLE STAPLE?

The FDA product code for COMPRESSION STAPLE AND SIMPLE STAPLE is JDR.

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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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