PROPEL
- Primary DI
- 30845854014831
- Brand
- PROPEL
- Company
- Conmed Corporation
- Model
- C8600
- Catalog number
- C8600
- Device description
- 9 MM X 20 MM PROPEL CANNULATED INTERFERENCE SCREW
- Published
- 2024-04-05
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
conmed.comProduct Codes#
| Code | Name |
|---|---|
| HWC | Screw, fixation, bone |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K874676 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30845854014831 | Package | GS1 | 1 | In Commercial Distribution |
| 10845854014837 | Previous | GS1 | 0 | |
| 20845854014834 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 30845854014831 | 30845854014831 |
| 10845854014837 | 10845854014837 |
| 20845854014834 | 20845854014834 |
GMDN Terms#
| Term | Definition |
|---|---|
| Tendon/ligament bone anchor, non-bioabsorbable | A non-bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)]. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | KEEP DRY |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(866)426-6633 | CustomerExperience@conmed.com |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
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|---|---|---|---|---|
| 20845854082482 | Paradigm | PEZS01A | PEZS01A | 2020-11-16 |
| 20845854015466 | SEQUENT | MR007C | MR007C | 2015-10-24 |
| 20845854036584 | SEQUENT | MR004C | MR004C | 2015-10-24 |
| 10653405044703 | CORE DYNAMICS | CD1406 | CD1406 | 2026-03-23 |
| 10653405045083 | CORE DYNAMICS | CD1608FH | CD1608FH | 2026-03-24 |
| 20653405990908 | GENESYS™ CrossFT™ | CFBC-4502R | CFBC-4502R | 2026-07-31 |
| 20653405990915 | GENESYS™ CrossFT™ | CFBC-4503R | CFBC-4503R | 2026-07-31 |
| 20653405990922 | GENESYS™ CrossFT™ | CFBC-5502R | CFBC-5502R | 2026-07-31 |
| 20653405990939 | GENESYS™ CrossFT™ | CFBC-5503R | CFBC-5503R | 2026-07-31 |
| 20653405990946 | GENESYS™ CrossFT™ | CFBC-6502R | CFBC-6502R | 2026-07-31 |
| 20653405990953 | GENESYS™ CrossFT™ | CFBC-6503R | CFBC-6503R | 2026-07-31 |
| 10653405000242 | YANKAUER | 0034470 | 0034470 | 2016-09-24 |
| 10845854035559 | E9000 | E9015 | E9015 | 2026-03-24 |
| 20653405008559 | CONMED | 60-0824-001 | 60-0824-001 | 2016-09-24 |
| 30653405003230 | CONMED | 138011 | 138011 | 2016-09-24 |
| 30653405003247 | CONMED | 138012 | 138012 | 2016-09-24 |
| 30653405058230 | AER DEFENSE | 60-8084-001 | 60-8084-001 | 2016-09-24 |
| 30845854655492 | PlumeSafe® X5™ | PX5-1354-22 | PX5-1354-22 | 2026-07-23 |
| 20845854042004 | Y-KNOT | YH01 | YH01 | 2015-10-24 |
| 20845854042028 | Y-KNOT | YH02 | YH02 | 2015-10-24 |
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