TRIANGLE SLING
FDA 510(k) clearance K980482 · decided 1998-03-27
Clearance details
- K-number
- K980482
- Device name
- TRIANGLE SLING
- Applicant
- Influence, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1998-02-09
- Decision date
- 1998-03-27
- Days to decision
- 46 days
- Clearance type
- Traditional
- Product code
- OTN
- Device class
- 2
- Regulation number
- 878.3300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- North Potomac, MD, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.