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FDA 510(k)

G-FORCE TI SUTURE ANCHOR SYSTEM

K-Number: K100579 · 2010-03-26

ApplicantWrightmedicaltechnologyinc
Decision Date2010-03-26
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

G-FORCE TI SUTURE ANCHOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2010-03-26 under 510(k) number K100579. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-FORCE TI SUTURE ANCHOR SYSTEM?

G-FORCE TI SUTURE ANCHOR SYSTEM is a medical device that received FDA 510(k) clearance on 2010-03-26. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K100579.

When did G-FORCE TI SUTURE ANCHOR SYSTEM receive FDA 510(k) clearance?

G-FORCE TI SUTURE ANCHOR SYSTEM received FDA 510(k) clearance on 2010-03-26, under 510(k) number K100579.

Who is the listed applicant for G-FORCE TI SUTURE ANCHOR SYSTEM?

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 G-FORCE TI SUTURE ANCHOR SYSTEM?

The FDA product code for G-FORCE TI SUTURE ANCHOR SYSTEM is MBI.

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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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