510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K771710Substantially Equivalent

Worrell Patella Template

Depuy, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771710 is the FDA 510(k) clearance record for WORRELL PATELLA TEMPLATE, a class I device, cleared for Depuy, Inc. on under FDA product code HWT (Template). FDA records list 67 510(k) clearances for Depuy, Inc., from to . As of , FDA records show no recalls naming K771710.

Clearance record

Decision date
Received
(24 days to decision)
Product code
HWT Template
Regulation
21 CFR 888.4800
Device class
Class I
Review panel
Orthopedic
Applicant
Depuy, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HWT

Trailing 12 months

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

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