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FDA 510(k)

BLADE ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K091936 · 2010-01-19

ApplicantNexxt Medical, Inc.
Decision Date2010-01-19
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLADE ANTERIOR CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nexxt Medical, Inc.. It received FDA 510(k) clearance on 2010-01-19 under 510(k) number K091936. 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 BLADE ANTERIOR CERVICAL PLATE SYSTEM?

BLADE ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-01-19. The listed applicant is Nexxt Medical, Inc.. The 510(k) number is K091936.

When did BLADE ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

BLADE ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2010-01-19, under 510(k) number K091936.

Who is the listed applicant for BLADE ANTERIOR CERVICAL PLATE SYSTEM?

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

What is the FDA product code for BLADE ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for BLADE ANTERIOR CERVICAL PLATE 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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