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FDA 510(k)

STIMULAN- CALCIUM SULFATE BONE VOID FILLER

K-Number: K982663 · 1999-02-26

ApplicantEncore Orthopedics, Inc.
Decision Date1999-02-26
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STIMULAN- CALCIUM SULFATE BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Encore Orthopedics, Inc.. It received FDA 510(k) clearance on 1999-02-26 under 510(k) number K982663. 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?

STIMULAN- CALCIUM SULFATE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 1999-02-26. The listed applicant is Encore Orthopedics, Inc.. The 510(k) number is K982663.

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

STIMULAN- CALCIUM SULFATE BONE VOID FILLER received FDA 510(k) clearance on 1999-02-26, under 510(k) number K982663.

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

The FDA 510(k) record lists Encore Orthopedics, Inc. 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?

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