Flower Small and Medium Bone Implants

FDA 510(k) K123562 · Flower Orthopedics Corporation

Substantially Equivalent

510(k) numberK123562

Submission

Device name
Flower Small and Medium Bone Implants
Applicant
Flower Orthopedics Corporation
Philedelphia, PA, US
Received
November 19, 2012
Decision date
March 29, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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More from Bonebridge AG

510(k)DeviceDecision
K192949Flower Suture Anchor SetMBI · Traditional 10/07/2020SE
K170687Flower Bone Screw SetHWC · Special 06/06/2017SE
K142306Flower Upper Extremity Plating SetHRS · Traditional 09/15/2014SE
K133930Flower Rear Foot Plating Set, Flower Calcaneus Planting Set, Flower Rearfoot Plating SetHRS · Traditional 03/27/2014SE
K133102Flower Ankle Plating SetHRS · Traditional 11/18/2013SE
K132248Flower Bone Screw SetHWC · Traditional 10/30/2013SE
K131657Flower Small and Medium Implant SetHRS · Special 08/22/2013SE

Questions and answers

When was Flower Small and Medium Bone Implants cleared by the FDA?

Flower Small and Medium Bone Implants (K123562) received a 510(k) decision of Substantially Equivalent on March 29, 2013, 130 days after the submission was received.

What is the product code of K123562?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.