LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
FDA 510(k) clearance K990212 · decided 1999-09-14
Clearance details
- K-number
- K990212
- Device name
- LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
- Applicant
- Doctor'S Research Group, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1999-01-22
- Decision date
- 1999-09-14
- Days to decision
- 235 days
- Clearance type
- Traditional
- Product code
- DYX
- Device class
- 2
- Regulation number
- 872.4600
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Wolcott, CT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.