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FDA 510(k)

RINGLOC + HYBRID ACETABULAR SYSTEM

K-Number: K093235 · 2010-04-30

ApplicantBiomet, Inc.
Decision Date2010-04-30
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RINGLOC + HYBRID ACETABULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2010-04-30 under 510(k) number K093235. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINGLOC + HYBRID ACETABULAR SYSTEM?

RINGLOC + HYBRID ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 2010-04-30. The listed applicant is Biomet, Inc.. The 510(k) number is K093235.

When did RINGLOC + HYBRID ACETABULAR SYSTEM receive FDA 510(k) clearance?

RINGLOC + HYBRID ACETABULAR SYSTEM received FDA 510(k) clearance on 2010-04-30, under 510(k) number K093235.

Who is the listed applicant for RINGLOC + HYBRID ACETABULAR SYSTEM?

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

What is the FDA product code for RINGLOC + HYBRID ACETABULAR SYSTEM?

The FDA product code for RINGLOC + HYBRID ACETABULAR SYSTEM is KWA.

Related Clinical Trials

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.

Other records listing Biomet, Inc. 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.

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Related Devices (Code: KWA)

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.

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