K-number	K093551
Device name	PARADIS VASO SHIELD
Applicant	Spinemedica, LLC
Product code	OMR
Device class	Class II
Decision date	Dec 24, 2009
Decision	Unknown
Regulation	870.3470

AI Summary

AI extraction for this record is queued and will appear within 24 hours. View full FDA record →

Source

View the full FDA submission: accessdata.fda.gov

Researching this as a predicate?

Want a transparent AI-ranking score, AI-discovered related predicates, ongoing safety and warning-letter monitoring, full predicate chain lineage, and a drafted SE rationale — all saved to your own project? That's what an account adds.

Start free trial →

Building an AI or ML-enabled device? Predicate search, PCCP tracking, and AI-specific FDA intelligence — built exclusively for AI/ML devices. Try AIFDA Intel →

PARADIS VASO SHIELD

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