Advanced Medical Technologies AG
Round Rock, TX, US
Advanced Medical Technologies AG appears in FDA device records in Round Rock, TX. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Advanced Medical Technologies AG between 2004 and 2012. The busiest year on record is 2012, with 4. The most recent is 2012, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2004 | 2 |
| 2005 | 1 |
| 2006 | 1 |
| 2008 | 1 |
| 2011 | 2 |
| 2012 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K121333 | WAVE D CAGE | MAX | Substantially Equivalent | |
| K121332 | LOOP CAGE | MAX | Substantially Equivalent | |
| K121330 | WAVE O CAGE | MAX | Substantially Equivalent | |
| K121288 | FUSE CAGE | MAX | Substantially Equivalent | |
| K103573 | ARTS2 SPINAL FIXATION SYSTEM | MNH | Substantially Equivalent | |
| K100945 | FUSE PLIF CAFE | MAX | Substantially Equivalent | |
| K080401 | SHELL CAGE, WAVE CAGE, LOOP CAGE | MAX | Substantially Equivalent | |
| K053473 | MAESTRO MDTL LASER SYSTEM | ILY | Substantially Equivalent | |
| K043353 | OMEGA EXCEL/XP LASER SYSTEM | NHN | Substantially Equivalent | |
| K033148 | ART ANTERIOR SPINAL SYSTEM | KWQ | Substantially Equivalent | |
| K033150 | ART POSTERIOR SPINAL SYSTEM | MNI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KWQAppliance, Fixation, Spinal Intervertebral Body
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- ILYLamp, Infrared, Therapeutic Heating
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- NHNPowered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain