K-number	K240347
Device name	PTG-05
Applicant	Zimmer Medizinsysteme GmbH
Product code	NGX
Device class	Class II
Decision date	Jul 21, 2024
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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PTG-05

Everything you need for a 510(k) submission. Nothing you don't.