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FDA 510(k)

CCG CERCLAGE SYSTEM

K-Number: K932024 · 1995-02-14

ApplicantEncore Orthopedics, Inc.
Decision Date1995-02-14
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

CCG CERCLAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Encore Orthopedics, Inc.. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K932024. 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 CCG CERCLAGE SYSTEM?

CCG CERCLAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Encore Orthopedics, Inc.. The 510(k) number is K932024.

When did CCG CERCLAGE SYSTEM receive FDA 510(k) clearance?

CCG CERCLAGE SYSTEM received FDA 510(k) clearance on 1995-02-14, under 510(k) number K932024.

Who is the listed applicant for CCG CERCLAGE SYSTEM?

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

What is the FDA product code for CCG CERCLAGE SYSTEM?

The FDA product code for CCG CERCLAGE SYSTEM is JDQ.

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Other records listing Encore Orthopedics, 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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