Simplify Disc— 510(k) K211757

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K211757 for Simplify Disc, Substantially Equivalent on 2021-08-20. Applicant: Nuvasive, Inc..

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code QLQ
Advisory panel: Orthopedic
Date received: 2021-06-07
Decision date: 2021-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

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