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FDA 510(k)

SEMIAL SPINAL IMPLANT

K-Number: K051659 · 2005-07-13

ApplicantSignus Medizintechnik GmbH
Decision Date2005-07-13
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEMIAL SPINAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Signus Medizintechnik GmbH. It received FDA 510(k) clearance on 2005-07-13 under 510(k) number K051659. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEMIAL SPINAL IMPLANT?

SEMIAL SPINAL IMPLANT is a medical device that received FDA 510(k) clearance on 2005-07-13. The listed applicant is Signus Medizintechnik GmbH. The 510(k) number is K051659.

When did SEMIAL SPINAL IMPLANT receive FDA 510(k) clearance?

SEMIAL SPINAL IMPLANT received FDA 510(k) clearance on 2005-07-13, under 510(k) number K051659.

Who is the listed applicant for SEMIAL SPINAL IMPLANT?

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

What is the FDA product code for SEMIAL SPINAL IMPLANT?

The FDA product code for SEMIAL SPINAL IMPLANT is MQP.

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Other records listing Signus Medizintechnik GmbH as applicant

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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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