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FDA 510(k)

ACROMED SCREW DRIVER

K-Number: K873066 · 1987-09-02

ApplicantBuckman Co., Inc.
Decision Date1987-09-02
Product CodeHXX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED SCREW DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1987-09-02 under 510(k) number K873066. The device is classified under product code HXX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED SCREW DRIVER?

ACROMED SCREW DRIVER is a medical device that received FDA 510(k) clearance on 1987-09-02. The listed applicant is Buckman Co., Inc.. The 510(k) number is K873066.

When did ACROMED SCREW DRIVER receive FDA 510(k) clearance?

ACROMED SCREW DRIVER received FDA 510(k) clearance on 1987-09-02, under 510(k) number K873066.

Who is the listed applicant for ACROMED SCREW DRIVER?

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

What is the FDA product code for ACROMED SCREW DRIVER?

The FDA product code for ACROMED SCREW DRIVER is HXX.

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Related Devices (Code: HXX)

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K901166DALTON TECHNOLOGY FLEXIBLE SCREWDRIVERDalton Technology, Inc.K872389PRECISION SCREW DRIVER SETMed-Tool, Inc.K8626892.5MM HEX DRIVER/CURVE PASSER/BONE PUNCH/RASPW. L. Gore & Associates, Inc.

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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