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Coaptite

FDA premarket approval P040047/S049 · decided 2018-02-12

Approval details

PMA number
P040047
Supplement
S049
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Coaptite
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Merz North America, Inc.
Date received
2018-01-16
Decision date
2018-02-12
Days to decision
27 days
Decision code
OK30
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Franksville, WI
Statement
Update to the test method for determining the pH of calcium hydroxyapatite (CaHA) particles.

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510(k) clearances by this applicant

RecordFirmDate
DESCRIBE PFD Patch (K172689)Merz North America, Inc.2017-11-29