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FDA 510(k)

ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM

K-Number: K875021 · 1987-12-30

ApplicantBuckman Co., Inc.
Decision Date1987-12-30
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM 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 1987-12-30 under 510(k) number K875021. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM?

ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Buckman Co., Inc.. The 510(k) number is K875021.

When did ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM receive FDA 510(k) clearance?

ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM received FDA 510(k) clearance on 1987-12-30, under 510(k) number K875021.

Who is the listed applicant for ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM?

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 AND ACE/FISCHER PRE-DRILL PIN SYSTEM?

The FDA product code for ACE AND ACE/FISCHER PRE-DRILL PIN SYSTEM is JDW.

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Related Devices (Code: JDW)

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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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