FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DYNAMATRIX

K Number: K082058 · Decision Oct 2, 2008
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
56
Applicant Total
31
Review Days
73

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Basic Information

Device Name
DYNAMATRIX
K Number
K082058
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Biotech, Inc.
Date Received
July 21, 2008
Decision Date
October 2, 2008
Product Code
NPL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NPL Barrier, Animal Source, Intraoral

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Other Clearances by Cook Biotech, Inc.

K Number Device Name
K133306 SIS HERNIA GRAFT
K133011 DIAPHRAGMATIC HERNIA GRAFT
K131015 BIODESIGN ONLAY DURAL GRAFT OR BIODESIGN DURAPLASTY GRAFT
K111695 HYBRID GRAFT
K110402 BIODESIGN NIPPLE RECONSTRUCTION CYLINDER
K090688 COOK UROLOGICAL GRAFT
K082682 SURGISIS BIODESIGN ENTEROCUTANEOUS FISTULA PLUG
K073391 SURGISIS BIODESIGN TISSUE GRAFT
K070405 MODIFICATION TO SURGISIS SLR STAPLE LINE REINFORCEMENT
K070738 SIS FACIAL CYLINDER, SIS FACIAL IMPLANT
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