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FDA 510(k)

CORSTREN COMPRESSION TUBE & PLATE

K-Number: K830196 · 1983-03-25

ApplicantZimmer, Inc.
Decision Date1983-03-25
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORSTREN COMPRESSION TUBE & PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1983-03-25 under 510(k) number K830196. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORSTREN COMPRESSION TUBE & PLATE?

CORSTREN COMPRESSION TUBE & PLATE is a medical device that received FDA 510(k) clearance on 1983-03-25. The listed applicant is Zimmer, Inc.. The 510(k) number is K830196.

When did CORSTREN COMPRESSION TUBE & PLATE receive FDA 510(k) clearance?

CORSTREN COMPRESSION TUBE & PLATE received FDA 510(k) clearance on 1983-03-25, under 510(k) number K830196.

Who is the listed applicant for CORSTREN COMPRESSION TUBE & PLATE?

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

What is the FDA product code for CORSTREN COMPRESSION TUBE & PLATE?

The FDA product code for CORSTREN COMPRESSION TUBE & PLATE is KTT.

Related Clinical Trials

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.

Other records listing Zimmer, Inc. as applicant

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.

View all 344 devices →

Related Devices (Code: KTT)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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