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FDA 510(k)

SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS

K-Number: K090686 · 2009-12-08

ApplicantSic Brevetti S.R.L.
Decision Date2009-12-08
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Sic Brevetti S.R.L.. It received FDA 510(k) clearance on 2009-12-08 under 510(k) number K090686. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS?

SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS is a medical device that received FDA 510(k) clearance on 2009-12-08. The listed applicant is Sic Brevetti S.R.L.. The 510(k) number is K090686.

When did SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS receive FDA 510(k) clearance?

SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS received FDA 510(k) clearance on 2009-12-08, under 510(k) number K090686.

Who is the listed applicant for SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS?

The FDA 510(k) record lists Sic Brevetti S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS?

The FDA product code for SIC BREVETTI S.R.L. DEVICE FOR STERNAL SYNTHESIS is JDQ.

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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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