510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K230850Substantially Equivalent

United Orthopedic Knee Patient Specific Instrumentation

Enhatch, Inc, Hasbrouck Heights NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K230850 is the FDA 510(k) clearance record for United Orthopedic Knee Patient Specific Instrumentation, a class II device, cleared for Enhatch, Inc. on under FDA product code OOG (Knee Arthroplasty Implantation System). FDA's definition for product code OOG reads: "Intended to be used to assist in the implantation of a specific knee arthroplasty device or a set of specific knee arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching...". FDA records list one 510(k) clearance for Enhatch, Inc. As of , FDA records show no recalls naming K230850.

Clearance record

Decision date
Received
(267 days to decision)
Product code
OOG Knee Arthroplasty Implantation System
Regulation
21 CFR 888.3560
Device class
Class II
Review panel
Orthopedic
Applicant
Enhatch, Inc. 226 Blvd., Hasbrouck Heights NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OOG

Trailing 12 months

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

FDA records show no clearances under product code OOG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OOG, 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