Ceboplane
510(k) K933933
Ceboplane is a Class I device made by Synvasive Technology, Inc., cleared under FDA 510(k) K933933 on 15 Apr 1994, active as of 22 Oct 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 | NumberK933933 | Date15 Apr 1994 | StatusActive |
Official records
- FDA 510(k) database K933933
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HTZ
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4800
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code HTZ (Instrument, Cutting, Orthopedic).
- Newclip Instruments ANC1105 by NEWCLIP TECHNICS
- NEW PODIATRY PRODUCTS by Dentronix, Inc.
- KAMBIN SPINAL INSTRUMENT SET by Pilling Co.
- Newclip Instruments ANC1432 by NEWCLIP TECHNICS
- Gimmi CA.1104.22 by Gimmi GmbH
- 5MM DOUGLE EDGE RING CURETTE by Stainless Mfg., Inc.
- MICRO OSCILLATING SAW by American Sterilizer Co.
- Gimmi CA.1140.27 by Gimmi GmbH
- BANANA KNIFE SERRATED by Stainless Mfg., Inc.
- CONCEPT SUCTION SLEEVE by Concept, Inc.