ALLOCRAFT DBM— 510(k) K052735

Substantially Equivalent

Lifecell Corp.

FDA 510(k) clearance K052735 for ALLOCRAFT DBM, Substantially Equivalent on 2005-12-28. Applicant: Lifecell Corp.. Device class: 2.

Clearance details

Applicant: Lifecell Corp.
Product code: Code MBP
Device class: Class 2
Regulation: 21 CFR 888.3045
Advisory panel: Orthopedic
Date received: 2005-09-30
Decision date: 2005-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.