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FDA 510(k)

MOBIS SPINAL IMPLANT

K-Number: K061082 · 2006-12-18

ApplicantSignus Medizintechnik GmbH
Decision Date2006-12-18
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOBIS 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 2006-12-18 under 510(k) number K061082. 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 MOBIS SPINAL IMPLANT?

MOBIS SPINAL IMPLANT is a medical device that received FDA 510(k) clearance on 2006-12-18. The listed applicant is Signus Medizintechnik GmbH. The 510(k) number is K061082.

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

MOBIS SPINAL IMPLANT received FDA 510(k) clearance on 2006-12-18, under 510(k) number K061082.

Who is the listed applicant for MOBIS 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 MOBIS SPINAL IMPLANT?

The FDA product code for MOBIS 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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