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FDA 510(k)

ARIZONA RADIO CAPITELLAR TOTAL ELBOW

K-Number: K812322 · 1982-01-04

ApplicantZimmer, Inc.
Decision Date1982-01-04
Product CodeJDB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARIZONA RADIO CAPITELLAR TOTAL ELBOW is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1982-01-04 under 510(k) number K812322. The device is classified under product code JDB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARIZONA RADIO CAPITELLAR TOTAL ELBOW?

ARIZONA RADIO CAPITELLAR TOTAL ELBOW is a medical device that received FDA 510(k) clearance on 1982-01-04. The listed applicant is Zimmer, Inc.. The 510(k) number is K812322.

When did ARIZONA RADIO CAPITELLAR TOTAL ELBOW receive FDA 510(k) clearance?

ARIZONA RADIO CAPITELLAR TOTAL ELBOW received FDA 510(k) clearance on 1982-01-04, under 510(k) number K812322.

Who is the listed applicant for ARIZONA RADIO CAPITELLAR TOTAL ELBOW?

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 ARIZONA RADIO CAPITELLAR TOTAL ELBOW?

The FDA product code for ARIZONA RADIO CAPITELLAR TOTAL ELBOW is JDB.

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: JDB)

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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