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

TEPHAFLEX MELTBLOWN CONSTRUCT

K Number: K130326 · Decision May 7, 2013
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
12
Applicant Total
18
Review Days
88

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Basic Information

Device Name
TEPHAFLEX MELTBLOWN CONSTRUCT
K Number
K130326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tepha, Inc.
Date Received
February 8, 2013
Decision Date
May 7, 2013
Product Code
OOD
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
OOD Surgical Film

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Other Clearances by Tepha, Inc.

K Number Device Name
K233999 GalaFLEX LITE Scaffold
K202425 SurgiLattice scaffold
K211307 GalaSTITCH Absorbable Monofilament Suture
K162922 GalaFORM 3D
K161092 GalaSHAPE 3D
K140533 GALAFLEX MESH
K132348 TEPHAFLEX BRAIDED SUTURE
K113721 TEPHAFLEX LIGHT MESH
K113723 TEPHAFLEX MESH
K111946 TEPHAFLEX MESH
Search all 18 clearances from Tepha, Inc. →