SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM— 510(k) K132740

Substantially Equivalent

Spinefrontier, Inc.

FDA 510(k) clearance K132740 for SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM, Substantially Equivalent on 2013-11-26. Applicant: Spinefrontier, Inc..

Clearance details

Applicant: Spinefrontier, Inc.
Product code: Code NQW
Advisory panel: Orthopedic
Date received: 2013-09-03
Decision date: 2013-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beverly, MA, US

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