510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K934582Substantially Equivalent for Some Indications

Gdlh Variable Angle Connector

Danek Group, Inc., Memphis TN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K934582 is the FDA 510(k) clearance record for GDLH VARIABLE ANGLE CONNECTOR, a class II device, cleared for Danek Group, Inc. on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 2 510(k) clearances for Danek Group, Inc., from to . As of , FDA records show no recalls naming K934582.

Clearance record

Decision date
Received
(271 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Danek Group, Inc. 3092 Directors Row, Memphis TN
Third party review
No

Clearances, product code KWP

Trailing 12 months

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

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