510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062391Substantially Equivalent

Disposable Posterior Lumbar Stabilization Procedure Kit, Models 9045-01 and 9045-02; Compression Tool, Model 6113-00

Triage Medical, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062391 is the FDA 510(k) clearance record for DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00, cleared for Triage Medical, Inc. on under FDA product code MRW (System, Facet Screw Spinal Device). FDA records list 11 510(k) clearances for Triage Medical, Inc., from to . As of , FDA records show one recall naming K062391.

Clearance record

Decision date
Received
(29 days to decision)
Product code
MRW System, Facet Screw Spinal Device
Device class
Unclassified
Review panel
Unknown
Applicant
Triage Medical, Inc. 13700 Alton Pkwy., Irvine CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRW

Trailing 12 months
7 clearances under product code MRW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MRW, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260