510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002082Substantially Equivalent

Speedlink Transverse Connector

Spinal Concepts, Inc., Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002082 is the FDA 510(k) clearance record for SPEEDLINK TRANSVERSE CONNECTOR, a class II device, cleared for Spinal Concepts, Inc. on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 46 510(k) clearances for Spinal Concepts, Inc., from to . As of , FDA records show 8 recalls naming K002082.

Clearance record

Decision date
Received
(88 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Spinal Concepts, Inc. 12012 Technology Blvd., #100, Austin TX
510(k) summary
Summary
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