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FDA 510(k)

CEMENT EXTRACTOR DRILL

K-Number: K770204 · 1977-02-08

ApplicantDepuy, Inc.
Decision Date1977-02-08
Product CodeHXY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CEMENT EXTRACTOR DRILL is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-02-08 under 510(k) number K770204. The device is classified under product code HXY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENT EXTRACTOR DRILL?

CEMENT EXTRACTOR DRILL is a medical device that received FDA 510(k) clearance on 1977-02-08. The listed applicant is Depuy, Inc.. The 510(k) number is K770204.

When did CEMENT EXTRACTOR DRILL receive FDA 510(k) clearance?

CEMENT EXTRACTOR DRILL received FDA 510(k) clearance on 1977-02-08, under 510(k) number K770204.

Who is the listed applicant for CEMENT EXTRACTOR DRILL?

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 CEMENT EXTRACTOR DRILL?

The FDA product code for CEMENT EXTRACTOR DRILL is HXY.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HXY)

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.

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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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