ClearanceBrief
Company ยท US

Additive Orthopaedics, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2022. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HRSPlate, Fixation, Bone5
HTYPin, Fixation, Smooth1
PBFOrthopaedic Surgical Planning And Instrument Guides1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 28, 2022K211076Patient Specific Marking Guides
Additive Orthopaedics, LLC
PBF
Jan 10, 2019K183011Additive Orthopaedics Patient Specific 3D Locking Lattice Plates
Additive Orthopaedics
HRS
May 16, 2018K180239Additive Orthopaedics Patient Specific 3D Printed Bone Segments
Additive Orthopaedics, LLC
HRS
Jun 20, 2017K163593Additive Orthopaedics Bunion System
Additive Orthopaedics, LLC
HRS
Apr 13, 2017K170214Additive Orthopaedics Locking Lattice Plate
Additive Orthopaedics, LLC
HRS
Sep 7, 2016K153207Additive Orthopaedics Bone Wedge System
Additive Orthopaedics, LLC
HRS
Jun 1, 2016K160264Additive Orthopaedics Hammertoe Correction System
Additive Orthopaedics, LLC
HTY

Latest recalls

DateFirm and productCodeLinked 510(k)
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