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FDA 510(k)

ORTHOPEDIC STOCKINETTE

K-Number: K770346 · 1977-03-07

ApplicantConvertors
Decision Date1977-03-07
Product CodeILG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Convertors. It received FDA 510(k) clearance on 1977-03-07 under 510(k) number K770346. The device is classified under product code ILG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC STOCKINETTE?

ORTHOPEDIC STOCKINETTE is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Convertors. The 510(k) number is K770346.

When did ORTHOPEDIC STOCKINETTE receive FDA 510(k) clearance?

ORTHOPEDIC STOCKINETTE received FDA 510(k) clearance on 1977-03-07, under 510(k) number K770346.

Who is the listed applicant for ORTHOPEDIC STOCKINETTE?

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

What is the FDA product code for ORTHOPEDIC STOCKINETTE?

The FDA product code for ORTHOPEDIC STOCKINETTE is ILG.

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 Convertors 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 10 devices →

Related Devices (Code: ILG)

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

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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