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FDA 510(k)

FISCHER WIRE/PIN CLAMP

K-Number: K860018 · 1986-02-07

ApplicantBuckman Co., Inc.
Decision Date1986-02-07
Product CodeHXK
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FISCHER WIRE/PIN CLAMP 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 1986-02-07 under 510(k) number K860018. The device is classified under product code HXK. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISCHER WIRE/PIN CLAMP?

FISCHER WIRE/PIN CLAMP is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Buckman Co., Inc.. The 510(k) number is K860018.

When did FISCHER WIRE/PIN CLAMP receive FDA 510(k) clearance?

FISCHER WIRE/PIN CLAMP received FDA 510(k) clearance on 1986-02-07, under 510(k) number K860018.

Who is the listed applicant for FISCHER WIRE/PIN CLAMP?

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 FISCHER WIRE/PIN CLAMP?

The FDA product code for FISCHER WIRE/PIN CLAMP is HXK.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: HXK)

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.

K890167HOLDER, NEEDLEDhason Brothers, Inc.K872989MICRINS NEEDLE HOLDERMicrins Surgical, Inc.K801594ACE FISCHER EXTERNAL FIXATION DEVICEAce Orthopedic Manufacturing Co.K772388CONVERSE-GILLIES NEEDLE HOLDEREdward Weck, Inc.

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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