DUNN ANTERIOR DISTRACTION SYSTEM— 510(k) K862755

Name: FDA 510(k) clearance K862755
Creator: U.S. Food and Drug Administration
Published: 1987-01-22

Substantially Equivalent for Some Indications

Osteotek, Inc.

FDA 510(k) clearance K862755 for DUNN ANTERIOR DISTRACTION SYSTEM, Substantially Equivalent for Some Indications on 1987-01-22. Applicant: Osteotek, Inc..

Clearance details

Applicant: Osteotek, Inc.
Advisory panel: Unknown
Date received: 1986-07-22
Decision date: 1987-01-22
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Salt Lake City, UT, US

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