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FDA 510(k)

NORIAN SRS BONE VOID FILLER

K-Number: K060408 · 2006-03-21

ApplicantSynthes (Usa)
Decision Date2006-03-21
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORIAN SRS 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 2006-03-21 under 510(k) number K060408. 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 SRS BONE VOID FILLER?

NORIAN SRS BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2006-03-21. The listed applicant is Synthes (Usa). The 510(k) number is K060408.

When did NORIAN SRS BONE VOID FILLER receive FDA 510(k) clearance?

NORIAN SRS BONE VOID FILLER received FDA 510(k) clearance on 2006-03-21, under 510(k) number K060408.

Who is the listed applicant for NORIAN SRS 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 SRS BONE VOID FILLER?

The FDA product code for NORIAN SRS BONE VOID FILLER is MQV.

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Related Devices (Code: MQV)

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.

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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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