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FDA 510(k)

ACE/FISCHER PERCUTANEOUS HALF PINS

K-Number: K875012 · 1988-01-14

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

Device Summary

ACE/FISCHER PERCUTANEOUS 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 K875012. 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/FISCHER PERCUTANEOUS HALF PINS?

ACE/FISCHER PERCUTANEOUS 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 K875012.

When did ACE/FISCHER PERCUTANEOUS HALF PINS receive FDA 510(k) clearance?

ACE/FISCHER PERCUTANEOUS HALF PINS received FDA 510(k) clearance on 1988-01-14, under 510(k) number K875012.

Who is the listed applicant for ACE/FISCHER PERCUTANEOUS 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/FISCHER PERCUTANEOUS HALF PINS?

The FDA product code for ACE/FISCHER PERCUTANEOUS HALF PINS 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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