Vitoss

Bone Graft Substitute, Foam Strip, Beta-Tricalcium Phosphate and Type I Bovine Collagen

Registry build 21.09.26
2manufacturers in China registered for this device type
29catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (1), Beijing (1).

Chinese manufacturers registered for FDA product code MQV
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Allgens Medical Technology Co., Ltd. Beijing Beijing Complaint-file establishment 1

Record

Regulatory record for Vitoss
Listed by Stryker GmbH, Switzerland
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K032288
Record published 2015-09-24
Record revised 2024-07-02 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Ambient; Special storage condition: Do Not Freeze; Storage environment temperature 15 to 25 °C; Special storage condition: Do Not Expose to Extreme Heat
Sizes Width 25 mm; height 4 to 8 mm; length 50 to 240 mm
Distribution end date 2024-07-04

Catalogue Numbers

Catalogue numbers for Vitoss
Catalogue number Size Status
2102-1110 Width 25.0 mm In distribution
2102-0020 Total Volume: 15.0 Cubic Centimeter In distribution
2102-1405 Total Volume: 5.0 Cubic Centimeter In distribution
2102-0010 Total Volume: 15.0 Cubic Centimeter In distribution
2102-0027 Total Volume: 10.0 Cubic Centimeter In distribution
2102-0033 Total Volume: 30.0 Cubic Centimeter In distribution
2102-0011 Total Volume: 30.0 Cubic Centimeter In distribution
2102-1105 Height 4.0 mm In distribution
2102-1402 Total Volume: 2.5 Cubic Centimeter In distribution
2102-0031 Total Volume: 10.0 Cubic Centimeter In distribution
2102-0009 Total Volume: 10.0 Cubic Centimeter In distribution
2102-0028 Total Volume: 15.0 Cubic Centimeter In distribution
2102-0016 Total Volume: 5.0 Cubic Centimeter In distribution
2102-1101 Length 240.0 mm In distribution
2102-0030 Total Volume: 5.0 Cubic Centimeter In distribution
2102-0029 Total Volume: 30.0 Cubic Centimeter In distribution
2102-1401 Total Volume: 1.2 Cubic Centimeter In distribution
2102-1120 Width 25.0 mm In distribution
2102-0026 Total Volume: 5.0 Cubic Centimeter In distribution
2102-1100 Total Volume: 10.0 Cubic Centimeter In distribution
2102-1410 Total Volume: 10.0 Cubic Centimeter In distribution
2102-0032 Total Volume: 15.0 Cubic Centimeter In distribution
2102-0015 Total Volume: 5.0 Cubic Centimeter In distribution
2102-1056 Total Volume: 23.0 Cubic Centimeter In distribution
2102-0021 Total Volume: 30.0 Cubic Centimeter In distribution
2102-0006 Total Volume: 10.0 Cubic Centimeter Withdrawn
2102-1310 Total Volume: 10.0 Cubic Centimeter Withdrawn
2102-0013 Total Volume: 1.2 Cubic Centimeter Withdrawn
2102-1305 Total Volume: 5.0 Cubic Centimeter Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Synthacer medArtis Medizinprodukte und Forschung Aktiengesellschaft 360
Syntricer medArtis Medizinprodukte und Forschung Aktiengesellschaft 357
Biosorb S.B.M 65
MagnetOs Kuros Biosciences B.V 61
BioSet® Rti Surgical, Inc. 47
Bicera® Resorbable Bone Substitute Wiltrom Corporation Limited 41
GRAFTON®and Grafton PLUS®Demineralized Bone Matrix (DBM) Medtronic Sofamor Danek, Inc. 40
Bicera® Resorbable Bone Substitute Wiltrom Co., Ltd. (Chutung) 39
ChronOS Synthes Gmbh 39
Synthacer/Syntricer medArtis Medizinprodukte und Forschung Aktiengesellschaft 36
Inion BioRestore™ Inion OY 35
Resorba Synthetic Bone Biomatlante 35

Showing 12 of 750. All products under Filler, Bone Void, Calcium Compound

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060061 2006-03-01

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