Atlas FDA

INFUSE BONE GRAFT

FDA premarket approval P050053/S022 · decided 2012-10-17

Approval details

PMA number
P050053
Supplement
S022
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INFUSE BONE GRAFT
Generic name
Bone grafting material, dental, with biologic component
Applicant
Medtronic, Inc.
Date received
2011-06-16
Decision date
2012-10-17
Days to decision
489 days
Decision code
APPR
Product code
NPZ
Advisory committee
Dental
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR CHANGE IN RESIN USAGE LIFETIME.

Class III intelligence, same tools

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

510(k) clearances by this applicant

RecordFirmDate
VitalFlow Set with Balance™ Biosurface (K261335)Medtronic, Inc.2026-07-31
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (K260195)Medtronic, Inc.2026-04-23
Retrograde Coronary Sinus Perfusion Cannulae (K253203)Medtronic, Inc.2026-02-19
Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
Bio-Medicus Life Support Catheter and Introducer (K251831)Medtronic, Inc.2026-01-15
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19