Atlas FDA

APLIGRAF

FDA premarket approval P950032/S072 · decided 2013-07-11

Approval details

PMA number
P950032
Supplement
S072
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
APLIGRAF
Generic name
Dressing, wound and burn, interactive
Applicant
Organogenesis, Inc.
Date received
2013-04-24
Decision date
2013-07-11
Days to decision
78 days
Decision code
APPR
Product code
MGR
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Canton, MA
Statement
APPROVAL FOR THE INTRODUCTION OF HUMAN EPIDERMAL KERATINOCYTE CELLSTRAIN 197 (HEP 197) FOR USE IN THE MANUFACTURE OF APLIGRAF, AND FOR APPROVAL OF A CHANGE FROM THE CURRENT TEST ASSAY FOR DETECTION OF CERTAIN VIRAL CONTAMINANTS TO A REAL-TIME PCR METHOD FROM A CONVENTIONAL GEL-BASED PCR METHOD.

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510(k) clearances by this applicant

RecordFirmDate
FortiShield (Biosynthetic Wound Matrix) (K212579)Organogenesis, Inc.2023-05-02
PuraPly Micronized Wound Matrix (PuraPly MZ) (K220317)Organogenesis, Inc.2022-07-01
FORTAGEN ORAL MEMBRANE (K071555)Organogenesis, Inc.2007-08-30
FORTADERM ANTIMICROBIAL WOUND DRESSING (K051647)Organogenesis, Inc.2005-11-08
CUFFPATCH (K042809)Organogenesis, Inc.2004-11-02
FORTAFLEX SURGICAL SLING (K021107)Organogenesis, Inc.2002-05-15
FORTAFLEX SURGICAL MESH (K021105)Organogenesis, Inc.2002-05-10
FORTAFLEX SURGICAL MESH (K020049)Organogenesis, Inc.2002-03-18