SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE
FDA 510(k) clearance K082828 · decided 2008-10-14
Clearance details
- K-number
- K082828
- Device name
- SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE
- Applicant
- Suturtek Incorporated
- Decision
- Substantially Equivalent
- Date received
- 2008-09-25
- Decision date
- 2008-10-14
- Days to decision
- 19 days
- Clearance type
- Special
- Product code
- GAQ
- Device class
- 2
- Regulation number
- 878.4495
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Acton, MA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Suturtek Incorporated
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.
Recalls involving this device
No recalls on record reference this clearance.