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FDA 510(k)

A/K SOCKET

K-Number: K802911 · 1980-12-17

ApplicantOrthomedics
Decision Date1980-12-17
Product CodeISS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

A/K SOCKET is the device name listed in this FDA 510(k) record. The listed applicant is Orthomedics. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802911. The device is classified under product code ISS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A/K SOCKET?

A/K SOCKET is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Orthomedics. The 510(k) number is K802911.

When did A/K SOCKET receive FDA 510(k) clearance?

A/K SOCKET received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802911.

Who is the listed applicant for A/K SOCKET?

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

What is the FDA product code for A/K SOCKET?

The FDA product code for A/K SOCKET is ISS.

Related Clinical Trials

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Other records listing Orthomedics 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.

K832742EXTENSION CONTROL KNEE ORTHOSISK832741JASON CERVICAL ORTHOSISK832740FEMORAL FRACTURE ORTHOSISK811456ORTHO-FRAC KITK811298EXECUTIVE COLLARK811297CERVICAL SUPPORT

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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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