FDA 510(k) Premarket Notification K112888: MESO WOUND MATRIX

Submission Details & Decision

Normalized public record details for 510(k) notification K112888.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K112888

Applicant / Sponsor

Kensey Nash Corporation

Device Name

MESO WOUND MATRIX

Product Code

KGN

Decision Date

2012-02-10

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Unknown ()

Clearance Type

Traditional

Third Party Flag

Date Received

2011-09-30

Related Establishments / Registrations

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