FDA 510(k) clearance · back to tracker

METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS

Biomet Manufacturing, Inc. cleared K113271 on 2012-05-18, decision: substantially equivalent

K-number

K113271

Sponsor

Biomet Manufacturing, Inc.

Device

METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS

Class

Class III

Decision

Substantially Equivalent

Decision date

2012-05-18

Product code

KWA

Advisory committee

Orthopedic

Medical specialty

Orthopedic

Regulation number

888.3330

Official FDA record

Open K113271on 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.

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Drop K113271 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.