TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX (K103033) — FDA 510(k) Clearance | Predicase

K-number	K103033
Device name	TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX
Applicant	Zimmer Trabecular Metal Technology
Product code	ODP
Device class	Class II
Decision date	Jan 10, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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