FREEMAN MODULAR HIP STEM RIDGED VERSION
K-Number: K890498 · 1989-10-13
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Device Summary
Frequently Asked Questions
What is the FREEMAN MODULAR HIP STEM RIDGED VERSION?
FREEMAN MODULAR HIP STEM RIDGED VERSION is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K890498.
When did FREEMAN MODULAR HIP STEM RIDGED VERSION receive FDA 510(k) clearance?
FREEMAN MODULAR HIP STEM RIDGED VERSION received FDA 510(k) clearance on 1989-10-13, under 510(k) number K890498.
Who is the listed applicant for FREEMAN MODULAR HIP STEM RIDGED VERSION?
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 FREEMAN MODULAR HIP STEM RIDGED VERSION?
The FDA product code for FREEMAN MODULAR HIP STEM RIDGED VERSION 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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