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FDA 510(k)

KESSELL TOTAL SHOULDER

K-Number: K770079 · 1977-01-25

Decision Date1977-01-25
Product Code
DecisionSubstantially Equivalent

Device Summary

KESSELL TOTAL SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1977-01-25 under 510(k) number K770079. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KESSELL TOTAL SHOULDER?

KESSELL TOTAL SHOULDER is a medical device that received FDA 510(k) clearance on 1977-01-25. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K770079.

When did KESSELL TOTAL SHOULDER receive FDA 510(k) clearance?

KESSELL TOTAL SHOULDER received FDA 510(k) clearance on 1977-01-25, under 510(k) number K770079.

Who is the listed applicant for KESSELL TOTAL SHOULDER?

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

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 Orthopedic Equipment Co., 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.

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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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