PRECICE System
K-Number: K172628 · 2017-09-25
Device Summary
Frequently Asked Questions
What is the PRECICE System?
PRECICE System is a medical device that received FDA 510(k) clearance on 2017-09-25. The listed applicant is Nuvasive Specialized Orthopedics, Inc.. The 510(k) number is K172628.
When did PRECICE System receive FDA 510(k) clearance?
PRECICE System received FDA 510(k) clearance on 2017-09-25, under 510(k) number K172628.
Who is the listed applicant for PRECICE System?
The FDA 510(k) record lists Nuvasive Specialized Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRECICE System?
The FDA product code for PRECICE System is HSB.
Other records listing Nuvasive Specialized Orthopedics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HSB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.