CONSENSUS CS2 PLUS ACETABULAR INSERT
K-Number: K100933 · 2010-10-06
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Device Summary
Frequently Asked Questions
What is the CONSENSUS CS2 PLUS ACETABULAR INSERT?
CONSENSUS CS2 PLUS ACETABULAR INSERT is a medical device that received FDA 510(k) clearance on 2010-10-06. The listed applicant is Consensus Orthopedics, Inc.. The 510(k) number is K100933.
When did CONSENSUS CS2 PLUS ACETABULAR INSERT receive FDA 510(k) clearance?
CONSENSUS CS2 PLUS ACETABULAR INSERT received FDA 510(k) clearance on 2010-10-06, under 510(k) number K100933.
Who is the listed applicant for CONSENSUS CS2 PLUS ACETABULAR INSERT?
The FDA 510(k) record lists Consensus Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONSENSUS CS2 PLUS ACETABULAR INSERT?
The FDA product code for CONSENSUS CS2 PLUS ACETABULAR INSERT is LPH.
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 Consensus Orthopedics, 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: LPH)
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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