FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

MP 719

K Number: K111524 · Decision Jul 22, 2011
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
41
Applicant Total
8
Review Days
50

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Basic Information

Device Name
MP 719
K Number
K111524
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Marine Polymer Technologies, Inc.
Date Received
June 2, 2011
Decision Date
July 22, 2011
Product Code
MTJ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MTJ Wax, Bone

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K Number Device Name
K160695 Talymed Suspension
K082703 MRDH BANDAGE
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K053300 SYVEKEXCEL
K002550 RDH BANDAGE
K984177 MODIFICATION TO SKVEKPATCH
K972914 SYVEK PATCH