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FDA 510(k)

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT

K-Number: K021551 · 2002-11-01

ApplicantBiocomposites, Ltd.
Decision Date2002-11-01
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Biocomposites, Ltd.. It received FDA 510(k) clearance on 2002-11-01 under 510(k) number K021551. 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 STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT?

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT is a medical device that received FDA 510(k) clearance on 2002-11-01. The listed applicant is Biocomposites, Ltd.. The 510(k) number is K021551.

When did STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT receive FDA 510(k) clearance?

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT received FDA 510(k) clearance on 2002-11-01, under 510(k) number K021551.

Who is the listed applicant for STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT?

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

What is the FDA product code for STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT?

The FDA product code for STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT is 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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