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FDA 510(k)

TOTAL KNEE PROSTHESIS-NONCONSTRAINED

K-Number: K771511 · 1977-11-30

Applicant3M Company
Decision Date1977-11-30
Product CodeHSX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TOTAL KNEE PROSTHESIS-NONCONSTRAINED is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1977-11-30 under 510(k) number K771511. The device is classified under product code HSX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOTAL KNEE PROSTHESIS-NONCONSTRAINED?

TOTAL KNEE PROSTHESIS-NONCONSTRAINED is a medical device that received FDA 510(k) clearance on 1977-11-30. The listed applicant is 3M Company. The 510(k) number is K771511.

When did TOTAL KNEE PROSTHESIS-NONCONSTRAINED receive FDA 510(k) clearance?

TOTAL KNEE PROSTHESIS-NONCONSTRAINED received FDA 510(k) clearance on 1977-11-30, under 510(k) number K771511.

Who is the listed applicant for TOTAL KNEE PROSTHESIS-NONCONSTRAINED?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOTAL KNEE PROSTHESIS-NONCONSTRAINED?

The FDA product code for TOTAL KNEE PROSTHESIS-NONCONSTRAINED is HSX.

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 3M Company 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: HSX)

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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