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FDA 510(k)

ORTHOTIC BRACING

K-Number: K761312 · 1977-01-10

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

Device Summary

ORTHOTIC BRACING 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 K761312. The device is classified under product code IQI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOTIC BRACING?

ORTHOTIC BRACING 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 K761312.

When did ORTHOTIC BRACING receive FDA 510(k) clearance?

ORTHOTIC BRACING received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761312.

Who is the listed applicant for ORTHOTIC BRACING?

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 ORTHOTIC BRACING?

The FDA product code for ORTHOTIC BRACING is IQI.

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.

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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.

K822632ELBOW PROSTHESISK821704FRACTURE BRACINGK801788HUMEROUS FRACTURE BRACE, ULNA FRACTUREK780891POST-OPERATIVE HIP ORTHOSISK780892FRACTURE BRACINGK780890CAPP TERMINAL DEVICE

View all 9 devices →

Related Devices (Code: IQI)

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.

K052771SENSOR WALKOtto Bock Healthcare LPK031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1Surgitech, Inc.K926391ACCUFLEX DYNAMIC ELBOW ORTHOSISRegulatory & Marketing Services, Inc.K910974MCCONNELL SHOULDER BRACEMcconnell OrthopedicK874502GAIT-AID ORTHOPEDIC INSOLEGait-Aid, Inc.K831542ADJUSTABLE POLYCENTRIC ELBOW HINGEFred Sammons, Inc.

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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