CREO® Stabilization System, REVERE® Stabilization System— 510(k) K181068
Substantially EquivalentGlobus Medical, Inc.
FDA 510(k) clearance K181068 for CREO® Stabilization System, REVERE® Stabilization System, Substantially Equivalent on 2018-06-29. Applicant: Globus Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Globus Medical, Inc.
- Product code
- Code PGM
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Audubon, PA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.