OMC ORTHOMET CANNULATED SCREW— 510(k) K862157

Substantially Equivalent

Orthomet, Inc.

FDA 510(k) clearance K862157 for OMC ORTHOMET CANNULATED SCREW, Substantially Equivalent on 1986-08-29. Applicant: Orthomet, Inc..

Clearance details

Applicant: Orthomet, Inc.
Advisory panel: Unknown
Date received: 1986-06-05
Decision date: 1986-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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