BIOMET CONCENTRIC HEX SCREW— 510(k) K781389

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K781389 for BIOMET CONCENTRIC HEX SCREW, Substantially Equivalent on 1978-08-21. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code JDO
Advisory panel: Orthopedic
Date received: 1978-08-10
Decision date: 1978-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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