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FDA 510(k)

ACE BEADED K-WIRES ACE OLIVE WIRES

K-Number: K895079 · 1989-09-13

ApplicantBuckman Co., Inc.
Decision Date1989-09-13
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE BEADED K-WIRES ACE OLIVE WIRES 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 1989-09-13 under 510(k) number K895079. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE BEADED K-WIRES ACE OLIVE WIRES?

ACE BEADED K-WIRES ACE OLIVE WIRES is a medical device that received FDA 510(k) clearance on 1989-09-13. The listed applicant is Buckman Co., Inc.. The 510(k) number is K895079.

When did ACE BEADED K-WIRES ACE OLIVE WIRES receive FDA 510(k) clearance?

ACE BEADED K-WIRES ACE OLIVE WIRES received FDA 510(k) clearance on 1989-09-13, under 510(k) number K895079.

Who is the listed applicant for ACE BEADED K-WIRES ACE OLIVE WIRES?

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 BEADED K-WIRES ACE OLIVE WIRES?

The FDA product code for ACE BEADED K-WIRES ACE OLIVE WIRES is HTY.

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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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