510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K120292Substantially Equivalent

Caplox II Pedicle Screw System

CAPTIVA SPINE, Inc., Apple Valley MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120292 is the FDA 510(k) clearance record for CAPLOX II PEDICLE SCREW SYSTEM, a class II device, cleared for Captiva Spine, Inc. on under FDA product code MNI (Orthosis, Spinal Pedicle Fixation). FDA records list 15 510(k) clearances for Captiva Spine, Inc., from to . As of , FDA records show one recall naming K120292.

Clearance record

Decision date
Received
(73 days to decision)
Product code
MNI Orthosis, Spinal Pedicle Fixation
Regulation
21 CFR 888.3070
Device class
Class II
Review panel
Orthopedic
Applicant
Captiva Spine, Inc. 13540 Guild Ave., Apple Valley MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNI

Trailing 12 months

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

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