Identity
- Trade Name
- PROPEL EUDAMEDFDA UDI
- Generic Name
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
- Device Name
- Orthopedic, Implant, Non-absorbable, Interference Screw, Titanium, Knee, Cannulated EUDAMEDPROPEL INTERFERENCE SCREW, 7 MM X 25 MM FDA UDI
- Model / Reference
- C8941 EUDAMEDFDA UDI
- Description
- PROPEL INTERFERENCE SCREW, 7 MM X 25 MM FDA UDI
Identifiers
- Catalog Number
- C8941 FDA UDI
- Primary DI / UDI-DI
- 20845854014957 EUDAMEDFDA UDI
- Basic UDI-DI
- B-20845854014957 EUDAMED
- 510(k) Number
- K933352 FDA UDI
- FDA Product Code
- HWC FDA UDI
- EMDN Code
- P09120605 INTERFERENCE SCREWS EUDAMED
- GMDN Term
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 25 Millimeter FDA UDI
Category: Tendon/ligament bone anchor, non-bioabsorbable
Propel by Conmed Corporation — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon/ligament bone anchor, non-bioabsorbable.
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- JuggerKnot Soft Anchors — Biomet Orthopedics, Inc. · Class II
- OrthoButton AL — RIVERPOINT MEDICAL LLC · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-20845854014957 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
- EUDAMED SRN
- US-MF-000012663
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (3)
- EUDAMED ccefb5f1-595f-4ee3-bacd-a19501ac41a3 61 fields · synced Jun 19, 2026
- FDA UDI 79c09938-c973-45b0-bb1e-eec42cdfec32 37 fields · synced May 30, 2026
- EUDAMED 3af06505-04b7-4c28-882a-aaa0f489eb4a 61 fields · synced Jun 19, 2026