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FDA 510(k)

ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM

K-Number: K963217 · 1996-10-02

ApplicantWrightmedicaltechnologyinc
Decision Date1996-10-02
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANCHORLOK II SOFT TISSUE 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 1996-10-02 under 510(k) number K963217. 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 ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM?

ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K963217.

When did ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM receive FDA 510(k) clearance?

ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM received FDA 510(k) clearance on 1996-10-02, under 510(k) number K963217.

Who is the listed applicant for ANCHORLOK II SOFT TISSUE 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 ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM?

The FDA product code for ANCHORLOK II SOFT TISSUE 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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