WATSON-FARRAR TOTAL HIP REPLACEMENT
K-Number: K770219 · 1977-02-17
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Device Summary
Frequently Asked Questions
What is the WATSON-FARRAR TOTAL HIP REPLACEMENT?
WATSON-FARRAR TOTAL HIP REPLACEMENT is a medical device that received FDA 510(k) clearance on 1977-02-17. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K770219.
When did WATSON-FARRAR TOTAL HIP REPLACEMENT receive FDA 510(k) clearance?
WATSON-FARRAR TOTAL HIP REPLACEMENT received FDA 510(k) clearance on 1977-02-17, under 510(k) number K770219.
Who is the listed applicant for WATSON-FARRAR TOTAL HIP REPLACEMENT?
The FDA 510(k) record lists Orthopedic Equipment Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WATSON-FARRAR TOTAL HIP REPLACEMENT?
The FDA product code for WATSON-FARRAR TOTAL HIP REPLACEMENT is JDG.
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 Equipment Co., 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: JDG)
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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