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

PORCINE SURGICAL MESH, PORCINE DERMAL MATRIX

K Number: K111436 · Decision Oct 14, 2011
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
3
Review Days
143

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Basic Information

Device Name
PORCINE SURGICAL MESH, PORCINE DERMAL MATRIX
K Number
K111436
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
Brennen Medical, LLC
Date Received
May 24, 2011
Decision Date
October 14, 2011
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

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Other Clearances by Brennen Medical, LLC

K Number Device Name
K113866 PORCINE DERMAL XENOGRAFTS PORCINE DERMAL MATRIX
K081272 PORCINE SURGICAL MESH; DERMAL MATRIX