FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

BIOMESH CA.B.S. 'AIR COMPOSITE, MODELS: CABST1R05T, CABSAIRC7, CABSAIRC09

K Number: K093196 · Decision Jun 25, 2010
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
6
Review Days
259

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Basic Information

Device Name
BIOMESH CA.B.S. 'AIR COMPOSITE, MODELS: CABST1R05T, CABSAIRC7, CABSAIRC09
K Number
K093196
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cousin Biotech Sas
Date Received
October 9, 2009
Decision Date
June 25, 2010
Product Code
FTL
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
FTL Mesh, Surgical, Polymeric

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Other Clearances by Cousin Biotech Sas

K Number Device Name
K181086 Cortical Fixation Systems
K181799 ResCUBE™ Ligament Fixation System
K172206 NAJA™ Ligament Correction System
K133889 PREMIUM
K072962 CABS'AIR