510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K882871Substantially Equivalent for Some Indications

Casf Drill Guide Dg 170

Terray Manufacturing, Inc., Ontario K7s 1l8, CA / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K882871 is the FDA 510(k) clearance record for CASF DRILL GUIDE DG 170, a class I device, cleared for Terray Manufacturing, Inc. on under FDA product code LYQ (Accessories, Fixation, Spinal Intervertebral Body). FDA records list 9 510(k) clearances for Terray Manufacturing, Inc., from to . As of , FDA records show no recalls naming K882871.

Clearance record

Decision date
Received
(74 days to decision)
Product code
LYQ Accessories, Fixation, Spinal Intervertebral Body
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
Terray Manufacturing, Inc. 24 Mcgonigal St. W., Ontario K7s 1l8, CA
Third party review
No

Clearances, product code LYQ

Trailing 12 months

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

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