Monterey AL Interbody System— 510(k) K201585
Substantially EquivalentStryker Corporation
FDA 510(k) clearance K201585 for Monterey AL Interbody System, Substantially Equivalent on 2020-08-10. Applicant: Stryker Corporation. Device class: 2.
Clearance details
- Applicant
- Stryker Corporation
- Product code
- Code OVD
- Device class
- Class 2
- Regulation
- 21 CFR 888.3080
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Allendale, NJ, US
Recent devices under product code OVD
view allMore clearances from Stryker Corporation
view all- K232157 — Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control
- K212194 — Stryker Q Guidance System with Cranial Guidance Software, CranialMask Tracker and Microscope Tracker, Passive Optical Navigation Instruments, Mayfield Base with Articulating Arm, and Navigated Biopsy Needle, Electromagnetic Navigation Instruments, Precision Targeting System
- K223770 — Sonopet 1Q 3 7cm 1Q Large
- K221728 — Aviator® Anterior Cervical Plating (ACP) System, LITe® Plate System, DynaTran Anterior Cervical Plating (ACP) System, Reflex Hybrid ACP System, UniVise Spinous Process Fixation Plate
- K221074 — OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device
Adverse events under product code OVD
product code OVD- Death
- 5
- Injury
- 495
- Total
- 500
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K201585
K-number listed on FDA's recall record- Z-1488-2025 — Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
- Z-1489-2025 — Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.
- Z-1490-2025 — Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.
- Z-1491-2025 — Monterey AL Implant Inserter; 22mm; Catalog 48019140.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K201585.
Data sourced from openFDA. This site is unofficial and independent of the FDA.