Vectorvision Hip
510(k) K010602
Vectorvision Hip is a medical device (FDA Class II; FDA product code HAW, Neurological Stereotaxic Instrument) made by Brainlab AG, cleared under FDA 510(k) K010602 on 12 Sep 2001, 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 | NumberK010602 | Date12 Sep 2001 | StatusActive |
Official records
- FDA 510(k) database K010602
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HAW
- Device class
- Class II
- Regulation
- 21 CFR Part 882.4560
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code HAW (Neurological Stereotaxic Instrument).
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- Zeta Cranial Navigation System (ZNS131-US) by ZETA SURGICAL INC.
- AXIEM IMAGELESS HIP MODULE FOR THE STEALTHSTATION SYSTEM by Medtronic Navigation Inc.
- Stealth AXiS Cranial Clinical Application by Medtronic Navigation Inc.
- SNT DISPOSABLE BIOPSY NEEDLE by Surgical Navigation Technologies, Inc.
- 6000-060-000 by Stryker Leibinger
- KELLY-GROERSS-KALL CT STEROTACTIC ADAPTATION SYS by Mayo Clinic