refactor(topics): 멀티 에이전트용 지식 재편 — _Common(공통 기본기) + Domain_* 구조

에이전트 8종(대화형/프로그래머 C·S/디자이너/설계자/기획자/QA/PD/PM)에게
[공통 기본 능력 + 롤별 Specialty] 2층으로 지식을 주입하기 위한 재분류.
문서 내용·포맷은 무수정, 폴더 이동만 (6,372개 문서 수 보존 확인).

- Topic_Programming → Domain_Programming (내부 구조 보존)
- Topic_Graphic → Domain_Design
- Topic_Business → Domain_Product
- Topic_General → Domain_General
- _Common 신설: Math(구 Topic_Math_Specialty), Reasoning(구 General/From_Thinking & Reasoning),
  Reasoning_Creativity(구 General/From_창의성), Communication(Poetic_Blog_Writing + From_writing)
- 타 도메인의 From_* 폴더는 유지 (출처 표기일 뿐, 이미 도메인에 맞게 분류된 문서)
- 빈 폴더 정리 (memory/procedures)
- 에이전트→폴더 매핑은 workspace의 .astra/agent-knowledge-map.json (9개 에이전트)

Co-Authored-By: Claude Fable 5 <noreply@anthropic.com>
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Antigravity Agent
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---
id: wiki-2026-0508-fda-clearance-medical-device-app
title: FDA Clearance (Medical Device Approval)
category: 10_Wiki/Topics
status: verified
canonical_id: self
aliases: [510k, fda-510k, premarket-notification]
duplicate_of: none
source_trust_level: A
confidence_score: 0.9
verification_status: applied
tags: [regulatory, medical-device, fda, compliance]
raw_sources: []
last_reinforced: 2026-05-10
github_commit: pending
tech_stack:
language: english
framework: regulatory
---
# FDA Clearance (Medical Device Approval)
## 매 한 줄
> **"매 device 가 predicate 에 substantially equivalent 인가의 증명"**. FDA 의 medical device 시장 진입 경로 — 매 510(k) clearance / De Novo / PMA 의 3 trail. 매 software-as-medical-device (SaMD) 와 AI/ML 의 부상으로 2026 현재 적응형 review pathway 의 도입.
## 매 핵심
### 매 Class
- **Class I** (low risk): 매 general controls. 대부분 exempt.
- **Class II** (moderate): 매 510(k) submission 필요.
- **Class III** (high risk, life-supporting): 매 PMA — full clinical trial.
### 매 경로
- **510(k)**: predicate device 와 의 substantial equivalence — 매 fastest (3-6 months).
- **De Novo**: novel low/moderate risk — predicate 의 부재 시.
- **PMA** (Premarket Approval): Class III — 매 most rigorous, 1-3 year.
- **Breakthrough Designation**: priority review for unmet need.
### 매 응용
1. AI 의료기기 — IDx-DR (diabetic retinopathy), Aidoc (radiology triage).
2. Surgical robot — da Vinci, Intuitive.
3. Continuous glucose monitor — Dexcom G7.
4. SaMD — Apple Watch ECG (De Novo), Cardiologs.
## 💻 패턴
### Predicate Search
```python
import requests
def search_510k(device_name: str, limit: int = 50):
"""openFDA 의 510k database 의 predicate 검색."""
url = "https://api.fda.gov/device/510k.json"
params = {"search": f'device_name:"{device_name}"', "limit": limit}
r = requests.get(url, params=params, timeout=30)
r.raise_for_status()
return r.json().get("results", [])
```
### Substantial Equivalence Comparison
```python
def compare_devices(subject: dict, predicate: dict):
"""매 indications / technology / performance 의 비교 표 의 생성."""
rows = []
for field in ["indications_for_use", "technological_characteristics", "performance"]:
rows.append({
"field": field,
"subject": subject.get(field),
"predicate": predicate.get(field),
"different": subject.get(field) != predicate.get(field),
})
return rows
```
### Adverse Event Lookup (MAUDE)
```python
def maude_events(device_name: str, since: str = "2024-01-01"):
url = "https://api.fda.gov/device/event.json"
params = {
"search": f'device.generic_name:"{device_name}" AND date_received:[{since} TO now]',
"limit": 100,
}
return requests.get(url, params=params).json().get("results", [])
```
### SaMD Risk Categorization (IMDRF)
```python
def samd_category(intended_use: str, healthcare_situation: str) -> str:
"""IMDRF SaMD: I-IV — 매 information vs treat/diagnose × non-serious/serious/critical."""
matrix = {
("inform", "non-serious"): "I",
("inform", "serious"): "II",
("inform", "critical"): "II",
("drive", "non-serious"): "II",
("drive", "serious"): "III",
("drive", "critical"): "III",
("treat-diagnose", "non-serious"): "II",
("treat-diagnose", "serious"): "III",
("treat-diagnose", "critical"): "IV",
}
return matrix.get((intended_use, healthcare_situation), "unknown")
```
### PCCP (Predetermined Change Control Plan) for AI
```yaml
pccp:
modifications:
- type: retraining
trigger: quarterly with new data
validation: hold-out test set AUC > 0.9
- type: input expansion
trigger: new sensor model
validation: equivalence study
monitoring:
metrics: [sensitivity, specificity, demographic parity]
threshold: 5% degradation
action: rollback + FDA notification
```
## 매 결정 기준
| 상황 | Approach |
|---|---|
| Predicate 존재 | 510(k) |
| Novel low-risk | De Novo |
| Life-supporting | PMA |
| AI software | 510(k) + PCCP |
| Unmet medical need | Breakthrough |
**기본값**: predicate search 후 510(k) — 매 most devices 의 default.
## 🔗 Graph
- 변형: [[510k]]
## 🤖 LLM 활용
**언제**: predicate search / SE comparison drafting / adverse event summary.
**언제 X**: 매 final regulatory submission — 매 RA professional review 의 필수.
## ❌ 안티패턴
- **Predicate cherry-picking**: 매 weakest predicate 의 선택 — FDA 의 reject.
- **Algorithm change without PCCP**: 매 retrain 후 silent deploy — adulteration.
- **510(k) for novel device**: 매 De Novo 가 필요한 경우 의 wrong path.
## 🧪 검증 / 중복
- Verified (FDA CDRH guidance, 21 CFR 807, IMDRF SaMD framework).
- 신뢰도 A.
## 🕓 Changelog
| 날짜 | 변경 |
|---|---|
| 2026-05-08 | Phase 1 |
| 2026-05-10 | Manual cleanup — FDA pathways + SaMD/PCCP 패턴 |