MOORE HIP PROSTHESIS FENESTRATED STEM
K-Number: K874616 · 1988-01-29
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Device Summary
Frequently Asked Questions
What is the MOORE HIP PROSTHESIS FENESTRATED STEM?
MOORE HIP PROSTHESIS FENESTRATED STEM is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K874616.
When did MOORE HIP PROSTHESIS FENESTRATED STEM receive FDA 510(k) clearance?
MOORE HIP PROSTHESIS FENESTRATED STEM received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874616.
Who is the listed applicant for MOORE HIP PROSTHESIS FENESTRATED STEM?
The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOORE HIP PROSTHESIS FENESTRATED STEM?
The FDA product code for MOORE HIP PROSTHESIS FENESTRATED STEM is JDI.
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 Orthopedic Systems, 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: JDI)
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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