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

Biodesign Parastomal Hernia Repair Graft

K Number: K162934 · Decision Jul 10, 2017
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
16
Review Days
263

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Biodesign Parastomal Hernia Repair Graft
K Number
K162934
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
Cook Biotech Incorporated
Date Received
October 20, 2016
Decision Date
July 10, 2017
Product Code
FTM
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
FTM Mesh, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Cook Biotech Incorporated

K Number Device Name
K232646 Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.6-0.9)
K201000 Biodesign Staple Line Reinforcement
K191696 Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft
K171817 Biodesign Diaphragmatic Hernia Graft
K170016 Biodesign Fistula Plug
K170945 Biodesign Staple Line Reinforcement
K161762 DynaMatrix/Dynamatrix Plus
K162741 AxoGuard Nerve Connector
K160136 Flowable Wound Matrix
K161221 Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
Search all 16 clearances from Cook Biotech Incorporated →