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FDA 510(k)

GRAVITYTM PEEK-OPTIMA Suture Anchor

K-Number: K170265 · 2017-02-23

Decision Date2017-02-23
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GRAVITYTM PEEK-OPTIMA Suture Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2017-02-23 under 510(k) number K170265. 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 GRAVITYTM PEEK-OPTIMA Suture Anchor?

GRAVITYTM PEEK-OPTIMA Suture Anchor is a medical device that received FDA 510(k) clearance on 2017-02-23. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K170265.

When did GRAVITYTM PEEK-OPTIMA Suture Anchor receive FDA 510(k) clearance?

GRAVITYTM PEEK-OPTIMA Suture Anchor received FDA 510(k) clearance on 2017-02-23, under 510(k) number K170265.

Who is the listed applicant for GRAVITYTM PEEK-OPTIMA Suture Anchor?

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 GRAVITYTM PEEK-OPTIMA Suture Anchor?

The FDA product code for GRAVITYTM PEEK-OPTIMA Suture Anchor is MBI.

Other records listing Wrightmedicaltechnologyinc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 37 devices →

Related Devices (Code: MBI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.