FDA 510(k) clearance · back to tracker

DYNASTY BIOFOAM SHELL

Wrightmedicaltechnologyinc cleared K121544 on 2012-07-30, decision: substantially equivalent

K-number

K121544

Sponsor

Wrightmedicaltechnologyinc

Device

DYNASTY BIOFOAM SHELL

Class

Class III

Decision

Substantially Equivalent

Decision date

2012-07-30

Product code

KWA

Advisory committee

Orthopedic

Medical specialty

Orthopedic

Regulation number

888.3330

Official FDA record

Open K121544on 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 K121544 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.

Try the sandbox

Source

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