FDA product code HSQ: Belt, Pelvic, Traction
HSQ is the FDA product code for belt, pelvic, traction. It is a Class I device, regulated under 21 CFR 888.5890 and reviewed by the Orthopedic panel. FDA has cleared 1 510(k) submission under HSQ. The average 510(k) review took 31 days (median 31).
Classification
| Field | Value |
|---|---|
| Device name | Belt, Pelvic, Traction |
| Device class | Class I |
| Regulation | 21 CFR 888.5890 |
| Review panel | OR — Orthopedic |
| Medical specialty | Orthopedic |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Compare with all 510(k) review times · Search every HSQ clearance
Top HSQ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Orthopedic Equipment Co., Inc. | 1 | 1976-12-16 |
Most recent HSQ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K761036 | Orthopedic Equipment Co., Inc. | WILSON SPINAL FRAME | 1976-12-16 | 31 |
Recalls for HSQ devices
openFDA lists no recalls for product code HSQ.
Frequently asked questions
What is FDA product code HSQ?
HSQ is the FDA product code for belt, pelvic, traction. It is a Class I device, regulated under 21 CFR 888.5890 and reviewed by the Orthopedic panel.
What device class is HSQ?
Class I, regulation 21 CFR 888.5890. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code HSQ?
Across 1 cleared submissions the average was 31 days from receipt to decision (median 31).
Which companies have the most HSQ clearances?
Orthopedic Equipment Co., Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code HSQ
- Run a recall and safety report across every HSQ manufacturer
- Watch product code HSQ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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