| Primary Device ID | M9703000062620200 | 
| NIH Device Record Key | aff9a0e9-0a35-4e5c-92fe-aca651e81726 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | DynaClip Forte | 
| Version Model Number | 3000-06-262020 | 
| Company DUNS | 601306413 | 
| Company Name | Medshape, Inc. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Unsafe | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | M9703000062620200 [Primary] | 
| JDR | Staple, Fixation, Bone | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
[M9703000062620200]
Radiation Sterilization
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-05-25 | 
| Device Publish Date | 2020-05-16 | 
| M9703000062620200 | DynaClip Forte Bone Fixation System, 26mm x 20mm x 20mm | 
| M9703000063020200 | DynaClip Forte Bone Fixation System, 30mm x 20mm x 20mm | 
| M97030000400000 | DYNACLIP PROCEDURE PACK, 4-LEG | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  DYNACLIP FORTE  88858769  not registered Live/Pending | MedShape, Inc. 2020-04-03 | 
|  DYNACLIP FORTE  88719509  not registered Live/Pending | MedShape, Inc. 2019-12-09 |