510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122378Substantially Equivalent

Nextgen Altius Oct System

Biomet Spine (Aka Ebi, LLC), Parsippany NJ / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122378 is the FDA 510(k) clearance record for NEXTGEN ALTIUS OCT SYSTEM, a class II device, cleared for Biomet Spine (Aka Ebi, LLC) on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 13 510(k) clearances for Biomet Spine (Aka Ebi, LLC), from to . As of , FDA records show one recall naming K122378.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Biomet Spine (Aka Ebi, LLC) 100 Interpace Pkwy., Parsippany NJ
510(k) summary
Summary PDF
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