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FDA 510(k)

SANTA CASA DISTRACTOR

K-Number: K791009 · 1979-06-11

ApplicantDepuy, Inc.
Decision Date1979-06-11
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SANTA CASA DISTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1979-06-11 under 510(k) number K791009. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANTA CASA DISTRACTOR?

SANTA CASA DISTRACTOR is a medical device that received FDA 510(k) clearance on 1979-06-11. The listed applicant is Depuy, Inc.. The 510(k) number is K791009.

When did SANTA CASA DISTRACTOR receive FDA 510(k) clearance?

SANTA CASA DISTRACTOR received FDA 510(k) clearance on 1979-06-11, under 510(k) number K791009.

Who is the listed applicant for SANTA CASA DISTRACTOR?

The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SANTA CASA DISTRACTOR?

The FDA product code for SANTA CASA DISTRACTOR is KWP.

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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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