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FDA 510(k)

CABLE-EASE PLATE AND CABLE SYSTEM

K-Number: K944529 · 1995-02-17

ApplicantIntermedics Orthopedics
Decision Date1995-02-17
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

CABLE-EASE PLATE AND CABLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1995-02-17 under 510(k) number K944529. 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 CABLE-EASE PLATE AND CABLE SYSTEM?

CABLE-EASE PLATE AND CABLE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-17. The listed applicant is Intermedics Orthopedics. The 510(k) number is K944529.

When did CABLE-EASE PLATE AND CABLE SYSTEM receive FDA 510(k) clearance?

CABLE-EASE PLATE AND CABLE SYSTEM received FDA 510(k) clearance on 1995-02-17, under 510(k) number K944529.

Who is the listed applicant for CABLE-EASE PLATE AND CABLE SYSTEM?

The FDA 510(k) record lists Intermedics Orthopedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CABLE-EASE PLATE AND CABLE SYSTEM?

The FDA product code for CABLE-EASE PLATE AND CABLE SYSTEM is 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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