510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K070274Substantially Equivalent

Echo Bi-Metric Press-Fit Stems

Biomet Manufacturing Corp, Warsaw IN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070274 is the FDA 510(k) clearance record for ECHO BI-METRIC PRESS-FIT STEMS, a class III device, cleared for Biomet Manufacturing Corp on under FDA product code KWA (Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)). FDA records list 128 510(k) clearances for Biomet Manufacturing Corp, from to . As of , FDA records show 3 recalls naming K070274.

Clearance record

Decision date
Received
(64 days to decision)
Product code
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Regulation
21 CFR 888.3330
Device class
Class III
Review panel
Orthopedic
Applicant
Biomet Manufacturing Corp P.O. Box 587, Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KWA

Trailing 12 months

FDA records hold no clearances under product code KWA in the trailing twelve months.

FDA records show no clearances under product code KWA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KWA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260