SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONS— 510(k) K073135

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K073135 for SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONS, Substantially Equivalent on 2008-01-29. Applicant: Synthes (Usa).

Clearance details

Applicant: Synthes (Usa)
Product code: Code LXT
Advisory panel: Orthopedic
Date received: 2007-11-07
Decision date: 2008-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

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