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FDA 510(k)

FX-CABLELOK CABLE/PLATE SYSTEM

K-Number: K935950 · 1994-03-09

ApplicantBuckman Co., Inc.
Decision Date1994-03-09
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

FX-CABLELOK CABLE/PLATE 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 1994-03-09 under 510(k) number K935950. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the FX-CABLELOK CABLE/PLATE SYSTEM?

FX-CABLELOK CABLE/PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is Buckman Co., Inc.. The 510(k) number is K935950.

When did FX-CABLELOK CABLE/PLATE SYSTEM receive FDA 510(k) clearance?

FX-CABLELOK CABLE/PLATE SYSTEM received FDA 510(k) clearance on 1994-03-09, under 510(k) number K935950.

Who is the listed applicant for FX-CABLELOK CABLE/PLATE 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 FX-CABLELOK CABLE/PLATE SYSTEM?

The FDA product code for FX-CABLELOK CABLE/PLATE SYSTEM is JDQ.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: JDQ)

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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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