K781343Substantially Equivalent

Resurface Proshesis

Name: K781343 Resurface Proshesis
Creator: Aesculap Instruments Corp.
Published: 1978-09-27
License: https://open.fda.gov/license/

Aesculap Instruments Corp., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K781343 is the FDA 510(k) clearance record for RESURFACE PROSHESIS, cleared for Aesculap Instruments Corp. on 1978-09-27. FDA records list 13 510(k) clearances for Aesculap Instruments Corp., from 1977-12-08 to 1990-02-28. As of 2026-09-10, FDA records show no recalls naming K781343.

Clearance record

Decision date: 1978-09-27
Received: 1978-08-04 (54 days to decision)
Review panel: Unknown
Applicant: Aesculap Instruments Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No