RINGLOC + HYBRID ACETABULAR SYSTEM
K-Number: K093235 · 2010-04-30
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Device Summary
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.
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
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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