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FDA 510(k)

4-BAR KNEE-SHIN SET-UP

K-Number: K761313 · 1977-01-10

ApplicantHosmer Dorrance Corp.
Decision Date1977-01-10
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

4-BAR KNEE-SHIN SET-UP is the device name listed in this FDA 510(k) record. The listed applicant is Hosmer Dorrance Corp.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K761313. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4-BAR KNEE-SHIN SET-UP?

4-BAR KNEE-SHIN SET-UP is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Hosmer Dorrance Corp.. The 510(k) number is K761313.

When did 4-BAR KNEE-SHIN SET-UP receive FDA 510(k) clearance?

4-BAR KNEE-SHIN SET-UP received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761313.

Who is the listed applicant for 4-BAR KNEE-SHIN SET-UP?

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

What is the FDA product code for 4-BAR KNEE-SHIN SET-UP?

The FDA product code for 4-BAR KNEE-SHIN SET-UP is ION.

Other records listing Hosmer Dorrance Corp. 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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Related Devices (Code: ION)

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

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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