Identity
- Trade Name
- QuickGraft FDA UDI
- Generic Name
- Tendon graft FDA UDI
- Device Name
- QuickGraft Pre-Sutured Tendon FDA UDI
- Model / Reference
- 430PST FDA UDI
- Description
- QuickGraft Pre-Sutured Tendon FDA UDI
Identifiers
- Catalog Number
- 430PST FDA UDI
- Primary DI / UDI-DI
- W41844300PSTT165 FDA UDI
- 510(k) Number
- K181633 FDA UDI
- FDA Product Code
- GAT FDA UDI
- GMDN Term
- Tendon graft FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5000 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
Yes
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Tendon graft
QuickGraft by Musculoskeletal Transplant Foundation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon graft.
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
- FlexiGRAFT® — LIFENET HEALTH · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Musculoskeletal Transplant Foundation
Sources (1)
- FDA UDI bd609b64-3d72-4cf7-b792-622a14d778c0 37 fields · synced Jun 6, 2026