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FDA 510(k)

CONDUIT Cages; FIBERGRAFT BG Putty

K-Number: K222276 · 2022-10-15

ApplicantDepuy Spine
Decision Date2022-10-15
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONDUIT Cages; FIBERGRAFT BG Putty is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Spine. It received FDA 510(k) clearance on 2022-10-15 under 510(k) 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. The listed applicant is Depuy Spine. The 510(k) number is K222276.

When did CONDUIT Cages; FIBERGRAFT BG Putty receive FDA 510(k) clearance?

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

Who is the listed applicant for CONDUIT Cages; FIBERGRAFT BG Putty?

The FDA 510(k) record lists Depuy Spine as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Depuy Spine as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: ODP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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