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FDA 510(k)

ACE BONE SCREW NUT

K-Number: K874669 · 1987-12-11

ApplicantBuckman Co., Inc.
Decision Date1987-12-11
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE BONE SCREW NUT 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 1987-12-11 under 510(k) number K874669. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE BONE SCREW NUT?

ACE BONE SCREW NUT is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Buckman Co., Inc.. The 510(k) number is K874669.

When did ACE BONE SCREW NUT receive FDA 510(k) clearance?

ACE BONE SCREW NUT received FDA 510(k) clearance on 1987-12-11, under 510(k) number K874669.

Who is the listed applicant for ACE BONE SCREW NUT?

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 ACE BONE SCREW NUT?

The FDA product code for ACE BONE SCREW NUT is HTN.

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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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