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FDA 510(k)

NORMED COMPRESSION BONE SCREW SYSTEM

K-Number: K032634 · 2003-10-06

ApplicantNoviace Corporation
Decision Date2003-10-06
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORMED COMPRESSION BONE SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Noviace Corporation. It received FDA 510(k) clearance on 2003-10-06 under 510(k) number K032634. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORMED COMPRESSION BONE SCREW SYSTEM?

NORMED COMPRESSION BONE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-06. The listed applicant is Noviace Corporation. The 510(k) number is K032634.

When did NORMED COMPRESSION BONE SCREW SYSTEM receive FDA 510(k) clearance?

NORMED COMPRESSION BONE SCREW SYSTEM received FDA 510(k) clearance on 2003-10-06, under 510(k) number K032634.

Who is the listed applicant for NORMED COMPRESSION BONE SCREW SYSTEM?

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

What is the FDA product code for NORMED COMPRESSION BONE SCREW SYSTEM?

The FDA product code for NORMED COMPRESSION BONE SCREW SYSTEM is JDS.

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Other records listing Noviace Corporation as applicant

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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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