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FDA 510(k)

POST-OPERATIVE HIP ORTHOSIS

K-Number: K780891 · 1978-06-13

ApplicantHosmer Dorrance Corp.
Decision Date1978-06-13
Product CodeITS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POST-OPERATIVE HIP ORTHOSIS 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 1978-06-13 under 510(k) number K780891. The device is classified under product code ITS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST-OPERATIVE HIP ORTHOSIS?

POST-OPERATIVE HIP ORTHOSIS is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Hosmer Dorrance Corp.. The 510(k) number is K780891.

When did POST-OPERATIVE HIP ORTHOSIS receive FDA 510(k) clearance?

POST-OPERATIVE HIP ORTHOSIS received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780891.

Who is the listed applicant for POST-OPERATIVE HIP ORTHOSIS?

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 POST-OPERATIVE HIP ORTHOSIS?

The FDA product code for POST-OPERATIVE HIP ORTHOSIS is ITS.

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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 FRACTUREK780890CAPP TERMINAL DEVICEK780892FRACTURE BRACINGK761314FLEXION-BRAKING KNEE-SHIN ASSEMBLY

View all 9 devices →

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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