Intellijoint HIP®

Magnetic, Inserter, Femoral Disc, Nails, G2

Registry build 21.09.26
5manufacturers in China registered for this device type
47catalogue numbers in this listing
6510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OLO
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for intellijoint HIP®
Listed by Intellijoint Surgical Inc., Canada
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Complaint-file establishment, Manufacturer, Exporter
510(k) K191507
Record published 2016-09-23
Record revised 2024-01-29 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number
Packaging Shelf box of 10
Distribution end date 2021-06-03

Catalogue Numbers

Catalogue numbers for intellijoint HIP®
Catalogue number Size Status
000-0209 In distribution
000-0387 In distribution
000-0373 In distribution
000-0163 In distribution
000-0251 In distribution
000-0210 In distribution
000-0241 In distribution
000-0172 In distribution
000-0202 In distribution
000-0272 In distribution
000-0284 In distribution
000-0280 In distribution
000-0393 In distribution
000-0250 In distribution
000-0206 In distribution
000-0377 In distribution
000-0159 In distribution
000-0214 In distribution
000-0356 In distribution
000-0208 In distribution
000-0368 In distribution
000-0207 In distribution
000-0161 In distribution
000-0247 In distribution
000-0401 In distribution
000-0249 In distribution
000-0366 In distribution
000-0211 In distribution
000-0358 In distribution
000-0160 In distribution
000-0283 In distribution
000-0234 In distribution
000-0189 In distribution
000-0229 In distribution
000-0158 In distribution
000-0260 In distribution
000-0152 In distribution
000-0190 In distribution
000-0233 In distribution
000-0300 In distribution
000-0252 In distribution
000-0282 In distribution
000-0197 In distribution
000-0285 In distribution
000-0275 Withdrawn
000-0270 Withdrawn
000-0376 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Valence Robotic Navigation System Alphatec Spine, Inc. 813
Olympic Astura Medical 684
Excelsius GPS Globus Medical, Inc. 383
Orthopedic Stereotaxic Instrument Medtronic Navigation, Inc. 356
Masada Astura Medical 335
Excelsiusgps Globus Medical, Inc. 297
Invictus Alphatec Spine, Inc. 235
OrthAlign Plus OrthAlign, Inc. 210
Arvis ® Kico Knee Innovation Company 174
OMNIBotics Omni Life Science, Inc. 150
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 137
Navigation Instruments VB Spine LLC 135

Showing 12 of 1,127. All products under Orthopedic Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K191507 2019-10-01
K172849 2017-11-16
K171525 2017-10-30
K162364 2017-03-02
K151364 2015-12-28
K133759 2014-07-23

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of intellijoint HIP®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Intellijoint Surgical Inc. 510(k) number 2020-02-11 Class II Software design During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth. 2020-06-10
Intellijoint Surgical Inc. 510(k) number 2019-06-28 Class II Nonconforming Material/Component Apple has determined that, in a limited number of older generation 15-inch MacBook Pro Units, the battery may overheat and pose a fire safety risk. To date, Intellijoint has distributed, 15-inch MacBook Pros which are the Workstation compo 23 units 2020-09-16

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer