Identity
- Trade Name
- Anchor Threaded Titanium FDA UDI
- Generic Name
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
- Device Name
- Threaded Ti 2x6mm 2 Suture, Needles, Drill FDA UDI
- Model / Reference
- ATT-2x6 2S ND FDA UDI
- Description
- Threaded Ti 2x6mm 2 Suture, Needles, Drill FDA UDI
Identifiers
- Catalog Number
- ATT-2x6 2S ND FDA UDI
- Primary DI / UDI-DI
- 06009712642731 FDA UDI
- 510(k) Number
- K212381 FDA UDI
- FDA Product Code
- MBI FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, non-bioabsorbable 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
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
Yes
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 2 Millimeter FDA UDI
Category: Tendon/ligament bone anchor, non-bioabsorbable
Anchor Threaded Titanium by Ortho-Design (pty) Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon/ligament bone anchor, non-bioabsorbable.
- Hi-Fi — Conmed Corporation · Class II
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- GII PANACRYL — DePuy Mitek, Inc. · Class II
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Cleared under the same submission
K212381 also covers:
- Anchor Impact PEEK — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded PEEK — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium-PEEK — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium-PEEK — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium-PEEK — ORTHO-DESIGN (PTY) LTD
- Anchor Threaded Titanium-PEEK — ORTHO-DESIGN (PTY) LTD
- DueLock — ORTHO-DESIGN (PTY) LTD
- MiniTi — ORTHO-DESIGN (PTY) LTD
- VersaPEEK — ORTHO-DESIGN (PTY) LTD
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
- Ortho-Design (pty) Ltd
Sources (1)
- FDA UDI 4cf76cf6-6ca7-45ff-b4ea-710bd24e20fc 37 fields · synced Jun 8, 2026