C-Plus
by Pioneer Surgical Technology Inc.
510(k) K133623
C-Plus is a Class II device made by Pioneer Surgical Technology Inc., cleared under FDA 510(k) K133623 on 10 Feb 2014, active as of 8 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK133623 | Date10 Feb 2014 | StatusActive |
Official records
- FDA 510(k) database K133623
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ODP
- FDA applicant
- Pioneer Surgical Technology, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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