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FDA 510(k)

TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM

K-Number: K953076 · 1997-02-28

ApplicantSofamor Danek USA,Inc.
Decision Date1997-02-28
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sofamor Danek USA,Inc.. It received FDA 510(k) clearance on 1997-02-28 under 510(k) number K953076. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM?

TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 1997-02-28. The listed applicant is Sofamor Danek USA,Inc.. The 510(k) number is K953076.

When did TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM receive FDA 510(k) clearance?

TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM received FDA 510(k) clearance on 1997-02-28, under 510(k) number K953076.

Who is the listed applicant for TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM?

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

What is the FDA product code for TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM?

The FDA product code for TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM is MRW.

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Other records listing Sofamor Danek USA,Inc. as applicant

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Related Devices (Code: MRW)

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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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