FDA 510(k) clearance · back to tracker

BIOMET MODULAR FEMORAL REVISION SYSTEM

Biomet, Inc. cleared K090757 on 2009-09-25, decision: substantially equivalent

K-number

K090757

Sponsor

Biomet, Inc.

Device

BIOMET MODULAR FEMORAL REVISION SYSTEM

Class

Class III

Decision

Substantially Equivalent

Decision date

2009-09-25

Product code

KWA

Advisory committee

Orthopedic

Medical specialty

Orthopedic

Regulation number

888.3330

Official FDA record

Open K090757on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K090757 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.