Identity
- Trade Name
- SF Push-in Anchor 2.3 FDA UDI
- Generic Name
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
- Model / Reference
- SF Push-in Anchor 2.3 FDA UDI
Identifiers
- Catalog Number
- B04-401 FDA UDI
- Primary DI / UDI-DI
- 07649990202167 FDA UDI
- FDA Product Code
- HWC FDA UDINKB FDA UDIMAI FDA UDIHTY FDA UDIGAT FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3070 FDA UDI888.3030 FDA UDI878.5000 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
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Width — 2.3 Millimeter FDA UDI
Category: Tendon/ligament bone anchor, bioabsorbable
SF Push-in Anchor 2.3 by Surgical Fusion Technologies GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon/ligament bone anchor, bioabsorbable.
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- HEALIX PEEK ORTHOCORD — Medos International Sàrl · Class II
- Arthrex® — Arthrex, Inc. · Class II
- 5 x 15mm CitreLock Implant — ACUITIVE TECHNOLOGIES · Class II
- Fix2Lock — OSTEONIC CO., Ltd. · Class II
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD. · Class II
- RIGIDFIX BIOCRYL — Medos International Sàrl · Class II
Cleared under the same submission
K171228 also covers:
K240288 also covers:
- Drill S-PI-A1.6 — Surgical Fusion Technologies GmbH
- Drill S-PI-A2.3 — Surgical Fusion Technologies GmbH
- Drill S-PI-A3.0 — Surgical Fusion Technologies GmbH
- Footswitch SupraFuser — Surgical Fusion Technologies GmbH
- Guide S-PI / W5.0 — Surgical Fusion Technologies GmbH
- Handpiece Front Cover — Surgical Fusion Technologies GmbH
- Handpiece SupraFuser — Surgical Fusion Technologies GmbH
- SF Push-in Anchor 1.6 — Surgical Fusion Technologies GmbH
- SF Push-in Anchor 3.0 — Surgical Fusion Technologies GmbH
- Sonotrode S-PI — Surgical Fusion Technologies GmbH
- Stopper S-PI-A1.6 — Surgical Fusion Technologies GmbH
- Stopper S-PI-A2.3 — Surgical Fusion Technologies GmbH
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
- Surgical Fusion Technologies GmbH
Sources (1)
- FDA UDI 843a0696-de34-43cb-be69-ed5e0f5f713c 37 fields · synced May 30, 2026