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APLIGRAF TM

FDA premarket approval P950032/S009 · decided 1999-04-19

Approval details

PMA number
P950032
Supplement
S009
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
APLIGRAF TM
Generic name
Dressing, wound and burn, interactive
Applicant
Organogenesis, Inc.
Date received
1999-03-25
Decision date
1999-04-19
Days to decision
25 days
Decision code
OK30
Product code
MGR
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Canton, MA
Statement
The 30-day Notice requested a manufacturing process change for Apligraf(TM). The requested change will place into the manufacturing process 3 additional production-scale incubators manufactured by Lunaire Corporation (model #CI0641W-6SPL).

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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