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

LTM-T SURGICAL MESH

K Number: K080353 · Decision Apr 3, 2008
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
10
Review Days
52

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Basic Information

Device Name
LTM-T SURGICAL MESH
K Number
K080353
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
Lifecell Corp.
Date Received
February 11, 2008
Decision Date
April 3, 2008
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 Lifecell Corp.

K Number Device Name
K130817 LTN - LAPAROSCOPIC SURGICAL MESH
K112534 LIFECELL TISSUE EXPANDER
K121289 LTM-LABAROSCOPIC SURGICAL MESH
K082176 LTM-BPS SURGICAL MESH
K082103 LTM WOUND DRESSING
K071986 LTM-RC SURGICAL MESH
K070560 LRTM SURGICAL MESH
K061208 LIFECELL DURAL SUBSTITUTE MATRIX
K052735 ALLOCRAFT DBM