FDA 510(k) clearance · back to tracker
PROFEMUR(R) E CEMENTLESS HIP STEM
Wrightmedicaltechnologyinc cleared K111698 on 2011-08-19, decision: substantially equivalent
K-number
K111698
Sponsor
Wrightmedicaltechnologyinc
Device
PROFEMUR(R) E CEMENTLESS HIP STEM
Class
Class III
Decision
Substantially Equivalent
Decision date
2011-08-19
Product code
KWA
Advisory committee
Orthopedic
Medical specialty
Orthopedic
Regulation number
888.3330
Official FDA record
Open K111698on 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 K111698 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 sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.