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FDA 510(k)

COMPRESSION SYSTEM

K-Number: K831076 · 1983-04-28

ApplicantKirschner Medical Corp.
Decision Date1983-04-28
Product CodeJDO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPRESSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831076. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSION SYSTEM?

COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K831076.

When did COMPRESSION SYSTEM receive FDA 510(k) clearance?

COMPRESSION SYSTEM received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831076.

Who is the listed applicant for COMPRESSION SYSTEM?

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

What is the FDA product code for COMPRESSION SYSTEM?

The FDA product code for COMPRESSION SYSTEM is JDO.

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Other records listing Kirschner Medical Corp. as applicant

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Related Devices (Code: JDO)

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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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