K-number	K911802
Device name	PMI (PATIENT MATCHED IMPLANTS) HIP FEMORAL COMP
Applicant	Biomet, Inc.
Product code	JDI
Device class	Class II
Decision date	Jan 2, 1992
Decision	Substantially Equivalent for Some Indications
Regulation	888.3350

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 →

PMI (PATIENT MATCHED IMPLANTS) HIP FEMORAL COMP

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