GetSet Surgical GoPLF! Posterior Lateral Fusion System
K-Number: K202505 · 2021-01-11
ApplicantGetset Surgical, SA
Decision Date2021-01-11
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
GetSet Surgical GoPLF! Posterior Lateral Fusion System is a medical device manufactured by Getset Surgical, SA. It received FDA 510(k) clearance on 2021-01-11 under approval number K202505. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the GetSet Surgical GoPLF! Posterior Lateral Fusion System?
GetSet Surgical GoPLF! Posterior Lateral Fusion System is a medical device that received FDA 510(k) clearance on 2021-01-11. It is manufactured by Getset Surgical, SA. The 510(k) number is K202505.
When was GetSet Surgical GoPLF! Posterior Lateral Fusion System approved by the FDA?
GetSet Surgical GoPLF! Posterior Lateral Fusion System received FDA 510(k) clearance on 2021-01-11, under approval number K202505.
What company makes GetSet Surgical GoPLF! Posterior Lateral Fusion System?
GetSet Surgical GoPLF! Posterior Lateral Fusion System is manufactured by Getset Surgical, SA.
What is the FDA product code for GetSet Surgical GoPLF! Posterior Lateral Fusion System?
The FDA product code for GetSet Surgical GoPLF! Posterior Lateral Fusion System is NKB.
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Official Source
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