K820218Substantially Equivalent

Pre-Sterilization of Vitallium Alloy

Name: K820218 Pre-Sterilization of Vitallium Alloy
Creator: Howmedica Corp.
Published: 1982-06-03
License: https://open.fda.gov/license/

Howmedica Corp., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K820218 is the FDA 510(k) clearance record for PRE-STERILIZATION OF VITALLIUM ALLOY, cleared for Howmedica Corp. on 1982-06-03. FDA records list 409 510(k) clearances for Howmedica Corp., from 1976-08-26 to 1999-02-24. As of 2026-09-10, FDA records show no recalls naming K820218.

Clearance record

Decision date: 1982-06-03
Received: 1982-01-26 (128 days to decision)
Review panel: Unknown
Applicant: Howmedica Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No