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FDA 510(k)

12-9170 SERIES II TOTAL HIP

K-Number: K761243 · 1976-12-16

Decision Date1976-12-16
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

12-9170 SERIES II TOTAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Richardo Manufacturing Co.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761243. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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