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FDA 510(k)

HA MCCUTCHEN SLT HIP SYSTEM

K-Number: K912452 · 1991-10-04

ApplicantDow Corning Wright
Decision Date1991-10-04
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HA MCCUTCHEN SLT HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K912452. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HA MCCUTCHEN SLT HIP SYSTEM?

HA MCCUTCHEN SLT HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Dow Corning Wright. The 510(k) number is K912452.

When did HA MCCUTCHEN SLT HIP SYSTEM receive FDA 510(k) clearance?

HA MCCUTCHEN SLT HIP SYSTEM received FDA 510(k) clearance on 1991-10-04, under 510(k) number K912452.

Who is the listed applicant for HA MCCUTCHEN SLT HIP SYSTEM?

The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HA MCCUTCHEN SLT HIP SYSTEM?

The FDA product code for HA MCCUTCHEN SLT HIP SYSTEM is MEH.

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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.

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