Identity
- Trade Name
- Grappler Suture Anchor System FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- Grappler ExO, ø4.75mm x 20mm Dynamic Knotless Anchor, Sterile Kit FDA UDI
- Model / Reference
- P82-240-4820-SK FDA UDI
- Description
- Grappler ExO, ø4.75mm x 20mm Dynamic Knotless Anchor, Sterile Kit FDA UDI
Identifiers
- Catalog Number
- P82-240-4820-SK FDA UDI
- Primary DI / UDI-DI
- 00889795128041 FDA UDI
- FDA Product Code
- MBI FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General internal orthopaedic fixation system implantation kit
Grappler Suture Anchor System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Paragon 28
Sources (1)
- FDA UDI 6e185399-717d-4b71-b082-56b99354dec0 34 fields · synced Jun 1, 2026