510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071243Substantially Equivalent

Metal Hemi Implant

Orthopro, LLC, Round Rock TX / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071243 is the FDA 510(k) clearance record for METAL HEMI IMPLANT, a class II device, cleared for Orthopro, LLC on under FDA product code KWD (Prosthesis, Toe, Hemi-, Phalangeal). FDA records list 7 510(k) clearances for Orthopro, LLC, from to . As of , FDA records show one recall naming K071243.

Clearance record

Decision date
Received
(20 days to decision)
Product code
KWD Prosthesis, Toe, Hemi-, Phalangeal
Regulation
21 CFR 888.3730
Device class
Class II
Review panel
Orthopedic
Applicant
Orthopro, LLC 1001 Oakwood Blvd., Round Rock TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KWD

Trailing 12 months
1 clearance under product code KWD in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KWD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260