510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110348Substantially Equivalent

Universal Clamp Spinal Fixation System

Zimmer Spine, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110348 is the FDA 510(k) clearance record for UNIVERSAL CLAMP SPINAL FIXATION SYSTEM, a class II device, cleared for Zimmer Spine on under FDA product code OWI (Bone Fixation Cerclage, Sublaminar). FDA's definition for product code OWI reads: "Acts as a bone anchor for temporary stabilization, or used in conjunction with other medical implants of similar metals when wiring is needed, during development of a spinal fusion". FDA records list 50 510(k) clearances for Zimmer Spine, from to . As of , FDA records show no recalls naming K110348.

Clearance record

Decision date
Received
(185 days to decision)
Product code
OWI Bone Fixation Cerclage, Sublaminar
Regulation
21 CFR 888.3010
Device class
Class II
Review panel
Orthopedic
Applicant
Zimmer Spine 7375 Bush Lake Rd., Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OWI

Trailing 12 months
2 clearances under product code OWI in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OWI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260