FREEMAN TOTAL HIP SYSTEM RIDGED STEM
K-Number: K890331 · 1989-10-13
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Device Summary
Frequently Asked Questions
What is the FREEMAN TOTAL HIP SYSTEM RIDGED STEM?
FREEMAN TOTAL HIP SYSTEM RIDGED STEM 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 K890331.
When did FREEMAN TOTAL HIP SYSTEM RIDGED STEM receive FDA 510(k) clearance?
FREEMAN TOTAL HIP SYSTEM RIDGED STEM received FDA 510(k) clearance on 1989-10-13, under 510(k) number K890331.
Who is the listed applicant for FREEMAN TOTAL HIP SYSTEM RIDGED 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 FREEMAN TOTAL HIP SYSTEM RIDGED STEM?
The FDA product code for FREEMAN TOTAL HIP SYSTEM RIDGED STEM is LWJ.
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: LWJ)
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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