Super Staple™ Classic

Product received FDA 510(k) clearance for: Hand and foot bone fragment and osteotomy fixation and joint arthrodesis, fixation of proximal tibial metaphysis osteotomy, and adjunctive…

Registry build 21.09.26

Product received FDA 510(k) clearance for: Hand and foot bone fragment and osteotomy fixation and joint arthrodesis, fixation of proximal tibial metaphysis osteotomy, and adjunctive fixation of small bone fragments (i.e. small fragments of bone that are not comminuted to the extent and preclude staple placement). These fragments may be located in long bones such as the femur, fibula or tibia in the lower extremities; the humerus, ulna or radius in the upper extremities; the clavicle and ribs, and in flat bone such as the pelvis, scapula and sternum. Pre-sterilized, all inclusive implant procedure tray contains; 1ea Nitinol bone staple implant of dimensions 25 x 25 x 25mm with a 2.0mm x 3.0mm diameter leg/bridge, 1ea pre-loaded staple delivery instrument with a lock pin, 1ea 25mm spaced drill guide; 2ea 1.5mm diameter Kirchner wire with protective tips; 2ea 3.0mm Pull Pins, 1ea 3.0mm Drill Bit (color band of purple).

7manufacturers in China registered for this device type
16catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Guangdong (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDR
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for Super Staple™ Classic
Listed by Metric Medical Devices, Inc., United States
FDA product code JDR
Device type Staple, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Manufacturer
Record published 2016-09-26
Record revised 2024-05-29 (version 4)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: Not subjected to storage or shipping temperatures in excess of 76.7°C (170°F)
Sizes Depth 7 to 30 mm; width 9 to 25 mm

Catalogue Numbers

Catalogue numbers for Super Staple™ Classic
Catalogue number Size Status
17001 13x10x10-1.5mm In distribution
21301 09x10x10-1.5mm In distribution
16601 Depth 07 mm In distribution
17101 Width 15 mm In distribution
22001 25x25x25-2×3 In distribution
17401 20x20x20-2.0mm In distribution
16801 11x10x10-1.5mm In distribution
21401 09x09x09-1.5 In distribution
22401 20x20x16-2×3 In distribution
16901 11x15x13-1.5 In distribution
21701 20x30x25-2×3 In distribution
21801 20×30-2×3 In distribution
21901 20x15x12-2×3 In distribution
17201 15x12x12-2.0mm In distribution
17501 20x20x20-2x3mm In distribution
17301 18x18x15-2.0mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DynaBridge Fusion Orthopedics, LLC 156
Arthrex® Arthrex, Inc. 80
Staple, Fixation, Bone Smith & Nephew, Inc. 59
Compression Staple System Tornier Inc. 36
UNI-Clip Newdeal Sas 35
Z-Staple Z-Medical Gmbh & Co. KG 34
Orbitum Staple System CPM Medical Consultants, LLC. 32
OSStaple Biomedical Enterprises, Inc. 30
Acumed Acumed LLC 30
Stealthfix Intraosseous Fixation System Medartis Inc. 29
Staple, Fixation, Bone Stryker GmbH 29
Step Boss Biomedical Enterprises, Inc. 27

Showing 12 of 319. All products under Staple, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K123363 2013-01-03

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