PUREGRAFT 50 SYSTEM— 510(k) K132815

Substantially Equivalent

Cytori Therapeutics, Inc.

FDA 510(k) clearance K132815 for PUREGRAFT 50 SYSTEM, Substantially Equivalent on 2014-01-24. Applicant: Cytori Therapeutics, Inc..

Clearance details

Applicant: Cytori Therapeutics, Inc.
Product code: Code MUU
Advisory panel: General, Plastic Surgery
Date received: 2013-09-09
Decision date: 2014-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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