LPC-PLUS ACETABULAR CUP
K-Number: K003274 · 2001-04-06
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Device Summary
Frequently Asked Questions
What is the LPC-PLUS ACETABULAR CUP?
LPC-PLUS ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 2001-04-06. The listed applicant is Plus Orthopedics. The 510(k) number is K003274.
When did LPC-PLUS ACETABULAR CUP receive FDA 510(k) clearance?
LPC-PLUS ACETABULAR CUP received FDA 510(k) clearance on 2001-04-06, under 510(k) number K003274.
Who is the listed applicant for LPC-PLUS ACETABULAR CUP?
The FDA 510(k) record lists Plus Orthopedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LPC-PLUS ACETABULAR CUP?
The FDA product code for LPC-PLUS ACETABULAR CUP is LZO.
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 Plus Orthopedics 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: LZO)
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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