Pisces-SA STANDALONE ALIF Interbody System— 510(k) K223413

Name: FDA 510(k) clearance K223413
Creator: U.S. Food and Drug Administration
Published: 2023-02-10

Substantially Equivalent

Osseus Fusion Systems

FDA 510(k) clearance K223413 for Pisces-SA STANDALONE ALIF Interbody System, Substantially Equivalent on 2023-02-10. Applicant: Osseus Fusion Systems. Device class: 2.

Clearance details

Applicant: Osseus Fusion Systems
Product code: Code OVD
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2022-11-09
Decision date: 2023-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OVD

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K261408 — SABER-XA System2026-08-03
K261809 — Interwedge® Standalone Lateral2026-07-31
K261353 — Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar Anchor System2026-07-15
K260810 — Anteralign LS coverplate2026-06-10
K254202 — MectaLIF 3D Metal Anterior2026-05-05

More clearances from Osseus Fusion Systems

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K222107 — Black Diamond POCT Spinal System2022-11-03
K213935 — PISCES-SA Standalone ALIF Interbody System2022-05-06
K192495 — Black Diamond Navigation Instruments2020-01-17
K192121 — Black Diamond Pedicle Screw System2019-10-29

Adverse events under product code OVD

product code OVD

Death: 5
Injury: 495
Total: 500

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.