Flower Orthopedics Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Flower Orthopedics Corporation - FDA 510(k) Cleared Devices
Recent clearances: Flower Suture Anchor Set
8
Total
8
Cleared
0
Denied
Flower Orthopedics Corporation has 8 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 8 cleared submissions from 2013 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Flower Orthopedics Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Flower Orthopedics Corporation
8 devices
Cleared
Oct 07, 2020
Flower Suture Anchor Set
Orthopedic
355d
Cleared
Jun 06, 2017
Flower Bone Screw Set
Orthopedic
91d
Cleared
Sep 15, 2014
Flower Upper Extremity Plating Set
Orthopedic
27d
Cleared
Mar 27, 2014
FLOWER REAR FOOT PLATING SET, FLOWER CALCANEUS PLANTING SET, FLOWER REARFOOT...
Orthopedic
94d
Cleared
Nov 18, 2013
FLOWER ANKLE PLATING SET
Orthopedic
49d
Cleared
Oct 30, 2013
FLOWER BONE SCREW SET
Orthopedic
103d
Cleared
Aug 22, 2013
FLOWER SMALL AND MEDIUM IMPLANT SET
Orthopedic
77d
Cleared
Mar 29, 2013
FLOWER SMALL AND MEDIUM BONE IMPLANTS
Orthopedic
130d