Quantum™* Flex 13-55-Pr-120
by Pioneer Surgical Technology Inc.
Quantum™* Flex 13-55-Pr-120 is a Class II device made by Pioneer Surgical Technology Inc., cleared under FDA 510(k) K101790 on 7 Mar 2011 and listed in FDA GUDID since 6 Nov 2015 (UDI-DI 00846468022389), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | GUDID listing | Number00846468022389 | Date6 Nov 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101790 | Date7 Mar 2011 | StatusActive |
Official records
- AccessGUDID record 00846468022389
- FDA 510(k) database K101790
Across registries
- FDA 510(k) K101790 decided 7 Mar 2011 Active
- FDA GUDID UDI-DI 00846468022389 listed 6 Nov 2015 Listed
Timeline
- Cleared FDA 510(k) K101790
- Listed FDA GUDID 00846468022389
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Quantum™* Flex
- Generic name
- Bone-screw internal spinal fixation system, non-sterile
- Model / reference
- 13-55-PR-120
- Primary DI / UDI-DI
- 00846468022389
- 510(k) Number
- FDA product code
- KWQ, KWP, NKB, MNI, MNH
- GMDN term
- Bone-screw internal spinal fixation system, non-sterile
- Device class
- Class II
- Regulation number
- 888.3060, 888.3050, 888.3070
- GUDID distribution status
- Not in Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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