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FDA 510(k)

FEMORAL CEMENT REMOVAL INSTRUMENT

K-Number: K840735 · 1984-05-14

ApplicantAmtech Scientific, Inc.
Decision Date1984-05-14
Product CodeHWX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FEMORAL CEMENT REMOVAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Amtech Scientific, Inc.. It received FDA 510(k) clearance on 1984-05-14 under 510(k) number K840735. The device is classified under product code HWX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL CEMENT REMOVAL INSTRUMENT?

FEMORAL CEMENT REMOVAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Amtech Scientific, Inc.. The 510(k) number is K840735.

When did FEMORAL CEMENT REMOVAL INSTRUMENT receive FDA 510(k) clearance?

FEMORAL CEMENT REMOVAL INSTRUMENT received FDA 510(k) clearance on 1984-05-14, under 510(k) number K840735.

Who is the listed applicant for FEMORAL CEMENT REMOVAL INSTRUMENT?

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

What is the FDA product code for FEMORAL CEMENT REMOVAL INSTRUMENT?

The FDA product code for FEMORAL CEMENT REMOVAL INSTRUMENT is HWX.

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Related Devices (Code: HWX)

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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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