510(k) K113528
- Device
- CLYDESDALE(R) SPINAL SYSTEM
- Applicant
- MEDTRONIC SOFAMOR DANEK USA, INC.
- 510(k) number
- K113528
- Product code
- MAX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2011-12-20
- Date received
- 2011-11-30
- Regulation
- 888.3080
- Classification name
- Intervertebral Fusion Device With Bone Graft, Lumbar
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- BECKY RONNER
- Address
- 1800 Pyramid Pl. Memphis TN US 38132 38132
FDA Registration Numbers#
- 3037407500
- 1724955
- 3010041430
- 3002807112
- 3006846753
- 1057425
- 3021006165
- 3009971621
- 3014967552
- 3006110997
- 3012429289
- 3016002322
- 3014725904
- 1030489
- 3015440604
- 3007014520
- 3004112448
- 1000493591
- 3013820501
- 1835251
- 1834331
- 3004638532
- 3005827567
- 3007024186
- 2183946
- 3010329663
- 9617297
- 3007766601
- 1835444
- 3009189869
- 1000461041
- 3005706667
- 3009882462
- 3010763958
- 3008102042
- 3019356409
- 3016261131
- 3013491327
- 1424434
- 3004641308
- 3013422238
- 3009217531
- 3003935342
- 1219655
- 3004976965
- 3009756327
- 3009169872
- 1833920
- 3011648620
- 3005562917
- 3005751028
- 3014937101
- 3007289746
- 3033509898
- 3010606097
- 3000170817
- 9611390
- 2531477
- 3005977257
- 3025603301
- 3009973699
- 3002807561
- 3017780544
- 3010370554
- 1833986
- 3011390763
- 3008599979
- 3015869493
- 9610612
- 3008868758
- 3010665091
- 1835296
- 3016050940
- 3009380063
- 3014257776
- 3010097171
- 2032521
- 3039167712
- 1935627
Source Documents#
Other 510(k) Records For Product Code MAX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K261430 | TruLift Expandable System | Life Spine, Inc. | 2026-07-28 |
| K253011 | Catalyft PL Expandable Interbody System | Medtronic Sofamor Danek USA, Inc. | 2026-07-17 |
| K261020 | Symmetrix™ L Spinal System | Medtronic Sofamor Danek USA, Inc. | 2026-07-14 |
| K253420 | Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody Sy | SeaSpine Orthopedics Corporation | 2026-07-01 |
| K253151 | Fule Interbody Fusion Cage System | Beijing Fule Science & Technology Development Co., Ltd. | 2026-06-15 |
| K261159 | Exceed® Biplanar Expandable Interbody System | Spine Wave, Inc. | 2026-05-29 |
| K253894 | BMD Titanium Spinal Fusion System | Global Biomedica s.r.o. | 2026-05-28 |
| K260506 | Ventana® P/T Lumbar Interbody System | Spinal Elements, Inc. | 2026-05-15 |
| K260837 | VersaLift Expandable System | Life Spine, Inc. | 2026-05-12 |
| K260385 | aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system | Carlsmed, Inc. | 2026-05-09 |
| K261067 | BEE PLIF Cage | NGMedical GmbH | 2026-04-30 |
| K254017 | SWINGO-3D Lumbar Cage System | Implanet | 2026-02-26 |
| K253583 | LUX Expandable Lumbar Interbody System | Xenix Medical | 2026-02-23 |
| K250773 | Luna® Ti Interbody Fusion System | Spinal Elements, Inc. | 2026-02-04 |
| K253748 | Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System | Life Spine, Inc. | 2026-01-23 |
Legacy Summary#
summary
FDA Review#
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