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

SEPRAMESH BIOSURGICAL COMPOSITE, MODEL SMBC-XXX

K Number: K994328 · Decision Mar 2, 2000
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
27
Review Days
71

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Basic Information

Device Name
SEPRAMESH BIOSURGICAL COMPOSITE, MODEL SMBC-XXX
K Number
K994328
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
Genzyme Corp.
Date Received
December 22, 1999
Decision Date
March 2, 2000
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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K021316 ULTRA N-GENEOUS HDL CHOLESTEROL REAGENT 1/REAGENT2; ULTRA N-GENEOUS HDL CHOLESTREOL CALIBRATOR
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