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FDA 510(k)

PRECICE STRYDE System

K-Number: K180503 · 2018-04-03

Decision Date2018-04-03
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRECICE STRYDE System is a medical device manufactured by Nuvasive Specialized Orthopedics, Inc.. It received FDA 510(k) clearance on 2018-04-03 under approval number K180503. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECICE STRYDE System?

PRECICE STRYDE System is a medical device that received FDA 510(k) clearance on 2018-04-03. It is manufactured by Nuvasive Specialized Orthopedics, Inc.. The 510(k) number is K180503.

When was PRECICE STRYDE System approved by the FDA?

PRECICE STRYDE System received FDA 510(k) clearance on 2018-04-03, under approval number K180503.

What company makes PRECICE STRYDE System?

PRECICE STRYDE System is manufactured by Nuvasive Specialized Orthopedics, Inc..

What is the FDA product code for PRECICE STRYDE System?

The FDA product code for PRECICE STRYDE System is HSB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.