12-9170 SERIES II TOTAL HIP
K-Number: K761243 · 1976-12-16
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Device Summary
Frequently Asked Questions
What is the 12-9170 SERIES II TOTAL HIP?
12-9170 SERIES II TOTAL HIP is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Richardo Manufacturing Co.. The 510(k) number is K761243.
When did 12-9170 SERIES II TOTAL HIP receive FDA 510(k) clearance?
12-9170 SERIES II TOTAL HIP received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761243.
Who is the listed applicant for 12-9170 SERIES II TOTAL HIP?
The FDA 510(k) record lists Richardo Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 12-9170 SERIES II TOTAL HIP?
The FDA product code for 12-9170 SERIES II TOTAL HIP 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.
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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