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FDA 510(k)

RESURFACE PROSHESIS

K-Number: K781343 · 1978-09-27

ApplicantAesculap Instruments Corp.
Decision Date1978-09-27
Product Code
DecisionSubstantially Equivalent

Device Summary

RESURFACE PROSHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Instruments Corp.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781343. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESURFACE PROSHESIS?

RESURFACE PROSHESIS is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K781343.

When did RESURFACE PROSHESIS receive FDA 510(k) clearance?

RESURFACE PROSHESIS received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781343.

Who is the listed applicant for RESURFACE PROSHESIS?

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

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Other records listing Aesculap Instruments 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.

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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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