510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K190670Substantially Equivalent

ORTHOLOC™ 2 Lapidus with Rotation System

Wrightmedicaltechnologyinc, Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K190670 is the FDA 510(k) clearance record for ORTHOLOC™ 2 Lapidus with Rotation System, a class II device, cleared for Wrightmedicaltechnologyinc on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 302 510(k) clearances for Wrightmedicaltechnologyinc, from to . As of , FDA records show no recalls naming K190670.

Clearance record

Decision date
Received
(60 days to decision)
Product code
HRS Plate, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Wrightmedicaltechnologyinc 1023 Cherry Rd., Memphis TN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HRS

Trailing 12 months
57 clearances under product code HRS in the twelve months to October 2026, March 2026 the highest month at 13.
Show the numbers
Monthly 510(k) clearances under FDA product code HRS, trailing twelve months
MonthClearances
November 20255
December 20255
January 20264
February 20265
March 202613
April 20266
May 20262
June 20265
July 20265
August 20263
September 20264
October 20260