Taiwan FDA registration 04e50669f4b4559aadf99374ce049907
"Avatek" Solos anterior lumbar intervertebral fusion system
TW: “阿伐泰克”索樂斯前路腰椎椎間融合系統
Taiwan·Risk Class 2·ALPHATEC SPINE INC.·Registered Dec 11, 2012 – Dec 11, 2022CancelledRegistration details
- Analysis ID
- 04e50669f4b4559aadf99374ce049907
- Customs Code
- DHA00602433306
Company information
- Manufacturer
- ALPHATEC SPINE INC.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- import
Dates and status
- Registration Date
- Dec 11, 2012
- Expiry Date
- Dec 11, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Avatek" Solos anterior lumbar intervertebral fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 04e50669f4b4559aadf99374ce049907 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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