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Arista AH; Arista AH Absorbable Hemostat

FDA premarket approval P050038/S032 · decided 2019-01-24

Approval details

PMA number
P050038
Supplement
S032
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Arista AH; Arista AH Absorbable Hemostat
Generic name
Agent, absorbable hemostatic, non-collagen based
Applicant
Davol, Inc.
Date received
2018-08-01
Decision date
2019-01-24
Days to decision
176 days
Decision code
APPR
Product code
LMG
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Warwick, RI
Statement
Approval for a new supplier of the subcomponent raw material HST (hydrolyzed starch technology) which is used in the manufacturing of the DSM-A (non-sterile powder) component of the Arista™ AH device. Additionally, the supplement includes an improvement in the test method for hydrolyzed starch characterization.

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