510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K130196Substantially Equivalent

Speedlock Knotless Fixation Device, 3Mm Drill, 3Mm+ Drill, Pathfinder Obturator & Sharp Tipped Obturator, Low Profile Dr

ArthroCare Corporation, Austin TX / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130196 is the FDA 510(k) clearance record for SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURATOR, LOW PROFILE DR, a class II device, cleared for Arthrocare Corp. on under FDA product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue). FDA records list 149 510(k) clearances for Arthrocare Corp., from to . As of , FDA records show no recalls naming K130196.

Clearance record

Decision date
Received
(30 days to decision)
Product code
MBI Fastener, Fixation, Nondegradable, Soft Tissue
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Arthrocare Corp. 2301 E Saint Elmo Rd. Suite 110, Austin TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MBI

Trailing 12 months
31 clearances under product code MBI in the twelve months to October 2026, March 2026 the highest month at 9.
Show the numbers
Monthly 510(k) clearances under FDA product code MBI, trailing twelve months
MonthClearances
November 20251
December 20252
January 20263
February 20261
March 20269
April 20261
May 20264
June 20261
July 20264
August 20262
September 20263
October 20260