FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

GluStitch Twist Tissue Adhesive

K Number: K150032 · Decision Jan 14, 2016
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
35
Applicant Total
5
Review Days
371

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Basic Information

Device Name
GluStitch Twist Tissue Adhesive
K Number
K150032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Glustitch, Inc.
Date Received
January 8, 2015
Decision Date
January 14, 2016
Product Code
MPN
Advisory Committee
General, Plastic Surgery
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
MPN Tissue Adhesive For The Topical Approximation Of Skin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MPN), ordered by most recent decision date.

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Other Clearances by Glustitch, Inc.

K Number Device Name
K083752 GLUSEAL 90, MODEL GLU9010
K071484 PERIACRYL 90,80,70,60, MODEL9010, 8020, 7030, 6040
K030574 GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSER
K013446 GLUSITE, MODEL GLU002