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FDA 510(k)

ACE/FISHER PERCUTANEOUS TRANSFIXING PINS

K-Number: K875022 · 1988-01-14

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

Device Summary

ACE/FISHER PERCUTANEOUS TRANSFIXING 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 K875022. 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/FISHER PERCUTANEOUS TRANSFIXING PINS?

ACE/FISHER PERCUTANEOUS TRANSFIXING 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 K875022.

When did ACE/FISHER PERCUTANEOUS TRANSFIXING PINS receive FDA 510(k) clearance?

ACE/FISHER PERCUTANEOUS TRANSFIXING PINS received FDA 510(k) clearance on 1988-01-14, under 510(k) number K875022.

Who is the listed applicant for ACE/FISHER PERCUTANEOUS TRANSFIXING 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/FISHER PERCUTANEOUS TRANSFIXING PINS?

The FDA product code for ACE/FISHER PERCUTANEOUS TRANSFIXING PINS is JDW.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: JDW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmBiodynamik, Inc.K250316Meduloc Intramedullary Fracture Fixation (IFF) SystemMeduloc, LLCK241357XT3 SystemBiodynamik, Inc.K223112MAVERICK Mini External Fixation SystemSmith & Nephew, Inc.K213874MAVERICK External Fixation SystemSmith & Nephew, Inc.K211508Steinmann Pins and Kirschner WiresStryker GmbH

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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