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FDA 510(k)

NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER

K-Number: K023862 · 2002-12-19

ApplicantSynthes (Usa)
Decision Date2002-12-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2002-12-19 under 510(k) number K023862. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER?

NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2002-12-19. The listed applicant is Synthes (Usa). The 510(k) number is K023862.

When did NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER receive FDA 510(k) clearance?

NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER received FDA 510(k) clearance on 2002-12-19, under 510(k) number K023862.

Who is the listed applicant for NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER?

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

What is the FDA product code for NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER?

The FDA product code for NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER is MQV.

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Related Devices (Code: MQV)

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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.

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