Identity
- Trade Name
- RAPIDLOC ETHIBOND FDA UDI
- Generic Name
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
- Device Name
- RAPIDLOC MENISCAL REPAIR-PLA TOPHAT / 0 Degrees Absorbable - PLA/PLA with Size 2/0 (3 metric) ETHIBOND Green braided polyester suture, and straight needle FDA UDI
- Model / Reference
- 228420 FDA UDI
- Description
- RAPIDLOC MENISCAL REPAIR-PLA TOPHAT / 0 Degrees Absorbable - PLA/PLA with Size 2/0 (3 metric) ETHIBOND Green braided polyester suture, and straight needle FDA UDI
Identifiers
- Catalog Number
- 228420 FDA UDI
- Primary DI / UDI-DI
- 10886705010240 FDA UDI
- 510(k) Number
- K002406 FDA UDI
- FDA Product Code
- GAS FDA UDIMAI FDA UDIGAM FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5000 FDA UDI888.3030 FDA UDI878.4493 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
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
Rapidloc Ethibond by DePuy Mitek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- DePuy Mitek, Inc.
Sources (1)
- FDA UDI 2c8b3df3-78f1-4e58-9c6e-6fb4ef48d947 38 fields · synced May 31, 2026