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FDA 510(k)

VERSABOND BONE CEMENT

K-Number: K001160 · 2000-12-11

ApplicantSmith & Nephew, Inc.
Decision Date2000-12-11
Product CodeLOD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERSABOND BONE CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2000-12-11 under 510(k) number K001160. The device is classified under product code LOD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSABOND BONE CEMENT?

VERSABOND BONE CEMENT is a medical device that received FDA 510(k) clearance on 2000-12-11. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K001160.

When did VERSABOND BONE CEMENT receive FDA 510(k) clearance?

VERSABOND BONE CEMENT received FDA 510(k) clearance on 2000-12-11, under 510(k) number K001160.

Who is the listed applicant for VERSABOND BONE CEMENT?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERSABOND BONE CEMENT?

The FDA product code for VERSABOND BONE CEMENT is LOD.

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Related Devices (Code: LOD)

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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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