FDA 510(k)

CONDUIT Cages; FIBERGRAFT BG Putty

K-Number: K222276 · 2022-10-15

Decision Date2022-10-15

Product CodeODP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CONDUIT Cages; FIBERGRAFT BG Putty is a medical device manufactured by Depuy Spine. It received FDA 510(k) clearance on 2022-10-15 under approval number K222276. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUIT Cages; FIBERGRAFT BG Putty?

CONDUIT Cages; FIBERGRAFT BG Putty is a medical device that received FDA 510(k) clearance on 2022-10-15. It is manufactured by Depuy Spine. The 510(k) number is K222276.

When was CONDUIT Cages; FIBERGRAFT BG Putty approved by the FDA?

CONDUIT Cages; FIBERGRAFT BG Putty received FDA 510(k) clearance on 2022-10-15, under approval number K222276.

What company makes CONDUIT Cages; FIBERGRAFT BG Putty?

CONDUIT Cages; FIBERGRAFT BG Putty is manufactured by Depuy Spine.

What is the FDA product code for CONDUIT Cages; FIBERGRAFT BG Putty?

The FDA product code for CONDUIT Cages; FIBERGRAFT BG Putty is ODP.

Related Clinical Trials

NCT06904898 CONDUIT vs. PEEK Cages ACTIVE_NOT_RECRUITING

Related Devices (Code: ODP)

K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

Official Source

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