VASOVASOSTOMY STABILIZER PLATFORM DEV— 510(k) K811223

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K811223 for VASOVASOSTOMY STABILIZER PLATFORM DEV, Substantially Equivalent on 1981-05-21. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code KOA
Advisory panel: Gastroenterology, Urology
Date received: 1981-05-04
Decision date: 1981-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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