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FDA 510(k)

FLEXION-BRAKING KNEE-SHIN ASSEMBLY

K-Number: K761314 · 1977-01-10

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

Device Summary

FLEXION-BRAKING KNEE-SHIN ASSEMBLY 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 K761314. 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 FLEXION-BRAKING KNEE-SHIN ASSEMBLY?

FLEXION-BRAKING KNEE-SHIN ASSEMBLY 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 K761314.

When did FLEXION-BRAKING KNEE-SHIN ASSEMBLY receive FDA 510(k) clearance?

FLEXION-BRAKING KNEE-SHIN ASSEMBLY received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761314.

Who is the listed applicant for FLEXION-BRAKING KNEE-SHIN ASSEMBLY?

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 FLEXION-BRAKING KNEE-SHIN ASSEMBLY?

The FDA product code for FLEXION-BRAKING KNEE-SHIN ASSEMBLY is ION.

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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

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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.

K120783ABLE-XIm-Able, Ltd.K885343STANDEXAlt, Inc.K851065GRAVITY KING (DEEMED SE 87/09/18)Unique Functional ProductsK840551MOBILIZERLossing Orthopedic, Inc.K833870KNEE WALKERMaddak, Inc.K833249FITNESSFitness Equipment Co., 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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