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FDA 510(k)

ACE PERCUTANEOUS 3MM HALF-PINS

K-Number: K875013 · 1988-01-14

ApplicantBuckman Co., Inc.
Decision Date1988-01-14
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE PERCUTANEOUS 3MM HALF-PINS 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 1988-01-14 under 510(k) number K875013. 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 PERCUTANEOUS 3MM HALF-PINS?

ACE PERCUTANEOUS 3MM HALF-PINS is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Buckman Co., Inc.. The 510(k) number is K875013.

When did ACE PERCUTANEOUS 3MM HALF-PINS receive FDA 510(k) clearance?

ACE PERCUTANEOUS 3MM HALF-PINS received FDA 510(k) clearance on 1988-01-14, under 510(k) number K875013.

Who is the listed applicant for ACE PERCUTANEOUS 3MM HALF-PINS?

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 PERCUTANEOUS 3MM HALF-PINS?

The FDA product code for ACE PERCUTANEOUS 3MM HALF-PINS is 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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