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FDA 510(k)

SYNTHES ANTERIOR CSLP SYSTEM

K-Number: K030866 · 2003-04-18

ApplicantSynthes (Usa)
Decision Date2003-04-18
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES ANTERIOR CSLP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2003-04-18 under 510(k) number K030866. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES ANTERIOR CSLP SYSTEM?

SYNTHES ANTERIOR CSLP SYSTEM is a medical device that received FDA 510(k) clearance on 2003-04-18. The listed applicant is Synthes (Usa). The 510(k) number is K030866.

When did SYNTHES ANTERIOR CSLP SYSTEM receive FDA 510(k) clearance?

SYNTHES ANTERIOR CSLP SYSTEM received FDA 510(k) clearance on 2003-04-18, under 510(k) number K030866.

Who is the listed applicant for SYNTHES ANTERIOR CSLP SYSTEM?

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 SYNTHES ANTERIOR CSLP SYSTEM?

The FDA product code for SYNTHES ANTERIOR CSLP SYSTEM is KWQ.

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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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