Tisuthes e-PTFE Surgical Patch
Summary
Shanghai Suokang Medical Implants Co., Ltd. received 510(k) clearance for Tisuthes e-PTFE Surgical Patch, a OWR device. Cleared on 2023-06-13.
Details
Source
510(k) Clearance
External ID
K201153
Action Date
2023-06-13
Status
Traditional
Category
device
Product Code
OWR
Product Description
Tisuthes e-PTFE Surgical Patch. Product code: OWR.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Shanghai Suokang Medical Implants Co., Ltd. have FDA actions?
This is the only FDA action we have on record for Shanghai Suokang Medical Implants Co., Ltd. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K201153" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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