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FDA 510(k)

Additive Orthopaedics Locking Lattice Plate

K-Number: K170214 · 2017-04-13

ApplicantAdditive Orthopaedics, LLC
Decision Date2017-04-13
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Additive Orthopaedics Locking Lattice Plate is a medical device manufactured by Additive Orthopaedics, LLC. It received FDA 510(k) clearance on 2017-04-13 under approval number K170214. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Additive Orthopaedics Locking Lattice Plate?

Additive Orthopaedics Locking Lattice Plate is a medical device that received FDA 510(k) clearance on 2017-04-13. It is manufactured by Additive Orthopaedics, LLC. The 510(k) number is K170214.

When was Additive Orthopaedics Locking Lattice Plate approved by the FDA?

Additive Orthopaedics Locking Lattice Plate received FDA 510(k) clearance on 2017-04-13, under approval number K170214.

What company makes Additive Orthopaedics Locking Lattice Plate?

Additive Orthopaedics Locking Lattice Plate is manufactured by Additive Orthopaedics, LLC.

What is the FDA product code for Additive Orthopaedics Locking Lattice Plate?

The FDA product code for Additive Orthopaedics Locking Lattice Plate is HRS.

Related PubMed Literature

PMID: 41166829 Assessment of intra-operative impact durability of additively manufactured mock lumbar intervertebral body fusion devices. Journal of biomechanics (2026)

Other Devices by Additive Orthopaedics, LLC

K153207Additive Orthopaedics Bone Wedge System K160264Additive Orthopaedics Hammertoe Correction System K163593Additive Orthopaedics Bunion System K180239Additive Orthopaedics Patient Specific 3D Printed Bone Segments K211076Patient Specific Marking Guides

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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