POSTURETEK
FDA 510(k) clearance K093553 · decided 2010-08-13
Clearance details
- K-number
- K093553
- Device name
- POSTURETEK
- Applicant
- Perseus Althetics,Llc
- Decision
- Substantially Equivalent
- Date received
- 2009-11-17
- Decision date
- 2010-08-13
- Days to decision
- 269 days
- Clearance type
- Traditional
- Product code
- LZW
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Perseus Althetics
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ZEGRA POSTURE TRAINER (K081540) | Peter Fischer | 2009-02-20 |
| SPINE TUNER POSTURE TRAINER (K951244) | Dan Kline | 1995-06-26 |
| BPA, BODY POSITION ALARM (K902669) | Bagrad | 1990-07-27 |
| MICRO-STRAIGHT POSTURE TRAINING DEVICE (K884976) | Mcdowell Ent., Inc. | 1989-06-09 |
Recalls involving this device
No recalls on record reference this clearance.