AVS PL PEEK SPACERS, MODELS 48351XXX AND 48353XXX (K073470) — FDA 510(k) Clearance | Predicase

K-number	K073470
Device name	AVS PL PEEK SPACERS, MODELS 48351XXX AND 48353XXX
Applicant	Stryker Spine
Product code	MAX
Device class	Class II
Decision date	Mar 6, 2008
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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