PLEXUR P— 510(k) K061982

Substantially Equivalent

Osteotech, Inc.

FDA 510(k) clearance K061982 for PLEXUR P, Substantially Equivalent on 2007-02-07. Applicant: Osteotech, Inc..

Clearance details

Applicant: Osteotech, Inc.
Product code: Code MBP
Advisory panel: Orthopedic
Date received: 2006-07-13
Decision date: 2007-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eatontown, NJ, US

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