Atlas FDA

AUGMENT BONE GRAFT

FDA premarket approval P100006/S004 · decided 2016-06-23

Approval details

PMA number
P100006
Supplement
S004
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AUGMENT BONE GRAFT
Generic name
Filler, bone void, synthetic peptide
Applicant
Biomimetic Therapeutics, LLC
Date received
2016-03-21
Decision date
2016-06-23
Days to decision
94 days
Decision code
APPR
Product code
NOX
Advisory committee
Orthopedic
Expedited review
No
Location
Franklin, TN
Statement
Approval for a manufacturing site located at BioMimetic Therapeutics, Inc. (BMTI), 389 Nichol Mill Lane, Franklin, Tennessee, for final kit assembly and packaging.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.