FDA 510(k)

PROSTHESIS, TOTAL HIP-RASP

K-Number: K760109 · 1976-07-20

Decision Date1976-07-20

Product CodeHTR

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, TOTAL HIP-RASP is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760109. The device is classified under product code HTR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHESIS, TOTAL HIP-RASP?

PROSTHESIS, TOTAL HIP-RASP is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K760109.

When did PROSTHESIS, TOTAL HIP-RASP receive FDA 510(k) clearance?

PROSTHESIS, TOTAL HIP-RASP received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760109.

Who is the listed applicant for PROSTHESIS, TOTAL HIP-RASP?

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 PROSTHESIS, TOTAL HIP-RASP?

The FDA product code for PROSTHESIS, TOTAL HIP-RASP is HTR.

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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.