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FDA 510(k)

VALEO PEDICLE SCREW SPINAL SYSTEM

K-Number: K072022 · 2007-11-19

ApplicantAmedica Corp.
Decision Date2007-11-19
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VALEO PEDICLE SCREW SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Amedica Corp.. It received FDA 510(k) clearance on 2007-11-19 under 510(k) number K072022. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALEO PEDICLE SCREW SPINAL SYSTEM?

VALEO PEDICLE SCREW SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-19. The listed applicant is Amedica Corp.. The 510(k) number is K072022.

When did VALEO PEDICLE SCREW SPINAL SYSTEM receive FDA 510(k) clearance?

VALEO PEDICLE SCREW SPINAL SYSTEM received FDA 510(k) clearance on 2007-11-19, under 510(k) number K072022.

Who is the listed applicant for VALEO PEDICLE SCREW SPINAL SYSTEM?

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

What is the FDA product code for VALEO PEDICLE SCREW SPINAL SYSTEM?

The FDA product code for VALEO PEDICLE SCREW SPINAL SYSTEM is NKB.

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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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